rs3736360
A SNP in the HSPG2 gene on chromosome 1. Its most notable genotype is C;T: Likely to be benign according to ClinVar
- Gene
- HSPG2
- Location
- Chr 121,823,627 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 16%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs3736360 on the minus strand: (A;G), (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.
- AverageC;T 25% C;C 71%
- European ancestry (Utah)C;T 30% C;C 64%
- Han Chinese (Beijing)C;T 25% C;C 72%
- Japanese (Tokyo)C;T 35% C;C 62%
- Yoruba (Nigeria)C;T 15% C;C 85%
- African ancestry (Southwest US)C;T 23% C;C 75%
- Chinese (Denver)C;T 32% C;C 66%
- Gujarati IndianC;T 29% C;C 57%
- Luhya (Kenya)C;T 19% C;C 81%
- Mexican ancestry (Los Angeles)C;T 32% C;C 65%
- Maasai (Kenya)C;T 14% C;C 84%
- TuscanC;T 26% C;C 65%
Related
Other HSPG2 SNPs
- rs137853248T;TSchwartz Jampel syndrome type 1Very important
- rs762281715A;ASchwartz Jampel syndrome type 1Very important
- rs778653296A;ASchwartz Jampel syndrome type 1Very important
- rs886039909T;TSchwartz Jampel syndrome type 1Very important
- rs886041667-;-Schwartz Jampel syndrome type 1Very important
- rs897471G;Gcommon in clinvarTypical
- rs989994C;Ccommon in complete genomicsTypical
- rs1874792T;Tcommon in clinvarTypical
Source and license
Adapted from rs3736360 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.