rs5030320
A SNP in the WT1 gene on chromosome 11. Its most notable genotype is T;T: common in clinvar
- Gene
- WT1
- Location
- Chr 1132,388,456 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, FamilyTreeDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs5030320 on the minus strand: (A;A). 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.
- AverageT;T 18%
- European ancestry (Utah)T;T 50%
- Han Chinese (Beijing)T;T 6%
- Japanese (Tokyo)T;T 12%
- Yoruba (Nigeria)T;T 5%
- African ancestry (Southwest US)T;T 5%
- Chinese (Denver)T;T 11%
- Gujarati IndianT;T 23%
- Luhya (Kenya)T;T 5%
- Mexican ancestry (Los Angeles)T;T 36%
- Maasai (Kenya)T;T 8%
- TuscanT;T 40%
Related
Other WT1 SNPs
- rs28941778C;TDenys-Drash syndromeVery important
- rs28941779A;GFrasier syndrome mutationVery important
- rs28942089A;GDenys-Drash syndromeVery important
- rs121907900A;GWilms tumor susceptibility (predicted)Very important
- rs121907906A;GWilms tumor susceptibility (predicted)Very important
- rs121907908C;TWilms tumor susceptibility (predicted)Very important
- rs121907909A;GWilms tumor susceptibility (predicted)Very important
- rs121907911G;TWilms tumor susceptibility (predicted)Very important
Source and license
Adapted from rs5030320 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.