rs9370096
A SNP in the PKHD1 gene on chromosome 6. Its most notable genotype is G;G: common in clinvar
- Gene
- PKHD1
- Location
- Chr 652,050,158 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 41%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageG;G 46%
- European ancestry (Utah)G;G 29%
- Han Chinese (Beijing)G;G 37%
- Japanese (Tokyo)G;G 43%
- Yoruba (Nigeria)G;G 80%
- African ancestry (Southwest US)G;G 67%
- Chinese (Denver)G;G 39%
- Gujarati IndianG;G 38%
- Luhya (Kenya)G;G 71%
- Mexican ancestry (Los Angeles)G;G 14%
- Maasai (Kenya)G;G 68%
- TuscanG;G 19%
Related
Other PKHD1 SNPs
- rs368263958A;AAutosomal recessive polycystic kidney diseaseVery important
- i5000044A;Apolycystic kidney diseaseVery important
- i5000046A;APolycystic kidney diseaseVery important
- rs28937907A;Apossible polycystic kidney diseaseVery important
- rs28939383A;APolycystic kidney diseaseVery important
- rs137852944A;APolycystic kidney diseaseVery important
- rs137852946T;Tpossible polycystic kidney diseaseVery important
- rs137852949A;APolycystic Kidney diseaseVery important
Notes
From SNPedia
Notes
Although a SNP in the PKHD1 gene, this variant is considered benign in ClinVar and not causative for any disorder.
Source and license
Adapted from rs9370096 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.