Genomics · Genetic Reports · Precision Wellness
Headaches & Migraines
Personalized Genetic Report
HeadachesMigraines
Accession #: MRW-26-3D6F96
Report type: Full Report
Report status: FINAL
Specimen and client information
Specimen type
Buccal (cheek) swab
Date reported
29 July 2026
Panel
Headaches & Migraines
What this report covers
Headaches · Migraines
About this report
This report reads your DNA and sorts every result into one of five plain-language groups, so you can see at a glance what deserves attention and what does not. Nothing here is a diagnosis. A flagged result means your genetics place you above or below the average person for that trait — a reason to ask a question, not a reason to worry.
What each result group means
Worth a conversation with your doctor
These came back with a higher genetic predisposition than most people. That is not a diagnosis — it means these are the ones worth raising at your next appointment.
Running above the typical range
Your genetics point to these sitting higher than average. Often useful to know, sometimes worth monitoring.
Running below the typical range
Your genetics point to these sitting lower than average. Same idea — context, not alarm.
Working in your favour
Good news. Your genetics look protective or better than average here.
In line with most people
Nothing unusual. These were tested and came back typical — worth having on record.
Your results at a glance
How to read this. A result being flagged does not mean you have a condition — it means your genetics put you above or below the average person for that trait. Of the 5 results here, 2 came back worth discussing with a clinician and 0 came back in your favour. Bring this document to your appointment.
Worth a conversation with your doctor (2)These came back with a higher genetic predisposition than most people. That is not a diagnosis — it means these are the ones worth raising at your next appointment.
From your Headaches & Migraines report
AMigraines
More likely
Higher predisposition than 99% of people
TRPM8 rs10166942 TT · IRAG1 rs4910165 GC · BDNF rs6265 TC · DHX36 rs13078967 AA · CARF rs138556413 CC · SLC24A3 rs4814864 CC · C12ORF4 rs2160875 CT
ACluster Headaches
More likely
Higher predisposition than 82% of people
SATB2 rs113658130 TC · UFL1 rs11153082 AG · ACOX3 rs532676091 CC · FAM83F rs147178151 GG · ZFHX4 rs143338229 CC · GLIS3 rs17701298 AA · FSHR rs150773296 GG · MPHOSPH6 rs74032638 GG
Running above the typical range (0)Your genetics point to these sitting higher than average. Often useful to know, sometimes worth monitoring.
Running below the typical range (0)Your genetics point to these sitting lower than average. Same idea — context, not alarm.
Working in your favour (0)Good news. Your genetics look protective or better than average here.
In line with most people (3)Nothing unusual. These were tested and came back typical — worth having on record.
From your Headaches & Migraines report
·Tension Headaches
Typical likelihood
In line with the general population · 64th percentile
TRPM8 rs10166942 TT · TRIM32 rs6478241 AA · HTR2A rs6313 GA · BDNF rs6265 TC · NOS3 rs2070744 TC · HNRNPA2B1 rs76473094 CC · TGFBR3 rs10493859 CA · CHSY3 rs17635642 CC
·Headache
Typical likelihood
In line with the general population · 51th percentile
HTR2A rs6313 GA · MTHFR rs1801133 AA · AOC1 rs2052129 GG · HNRNPA2B1 rs76473094 CC · TGFBR3 rs10493859 CA · CHSY3 rs17635642 CC · BTN3A2 rs2072806 CC · UFL1 rs9486715 AC
·DAO (Histamine)
Typical activity
In line with the general population
AOC1 rs1049793 GC · AOC1 rs1049742 CC · AOC1 rs2052129 GG
Methodology
Genotyping was performed on DNA extracted from a buccal (cheek) swab using a genome-wide array. Results are derived from peer-reviewed genome-wide association data and, where applicable, published clinical guidelines. Each report was scored independently against its own reference set. Percentile figures describe where your result sits relative to a reference population.
Limitations
This is a laboratory-developed test. It has not been cleared or approved by the U.S. Food and Drug Administration. Genotyping does not detect all variants in the genes assessed; the absence of a flagged result does not exclude risk. Predisposition is probabilistic and is modified by environment, lifestyle, ancestry and family history. Results must be interpreted by a qualified healthcare professional and must not be used alone to diagnose, treat, or alter any medication regimen. Marrow does not recommend, prescribe, or dose any supplement or medication.
Performing laboratory & attestation
| Performing laboratory | Gene by Gene, Ltd. |
| Laboratory address | 1445 North Loop West, Suite 760, Houston, TX 77008 |
| CLIA certification | CLIA #45D1102202 |
| CAP accreditation | CAP #7212851 · accredited through 7 October 2027 |
| Laboratory Director | Feng Zhou, PhD, MB(ASCP) |
| Specimen type | Buccal (cheek) swab — genomic DNA |
| Accession | MRW-26-3D6F96 |
| Date reported | 29 July 2026 |
This specimen was tested at Gene by Gene, Ltd., 1445 North Loop West, Suite 760, Houston, TX 77008, under CLIA #45D1102202 and CAP #7212851. Laboratory Director: Feng Zhou, PhD, MB(ASCP). Marrow Health is not a clinical laboratory and does not perform testing; Marrow prepares and delivers this report from data produced by the performing laboratory named above. Report generated 29 July 2026 · Accession MRW-26-3D6F96 · © 2026 Marrow Health.