rs2819590
A SNP in the SUMF1 gene on chromosome 3. Its most notable genotype is C;C: common in clinvar
- Gene
- SUMF1
- Location
- Chr 34,467,058 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, FamilyTreeDNA
- Minor allele frequency
- 14%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs2819590 on the minus strand: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageC;C 87%
- European ancestry (Utah)C;C 50%
- Han Chinese (Beijing)C;C 100%
- Japanese (Tokyo)C;C 100%
- Yoruba (Nigeria)C;C 98%
Related
Other SUMF1 SNPs
- rs137852844G;TCarrier of a multiple sulfatase deficiency mutationImportant
- rs137852845A;GCarrier of a multiple sulfatase deficiency mutationImportant
- rs137852846A;GCarrier of a multiple sulfatase deficiency mutationImportant
- rs137852847C;TCarrier of a multiple sulfatase deficiency mutationImportant
- rs137852848A;GCarrier of a multiple sulfatase deficiency mutationImportant
- rs137852849A;GCarrier of a multiple sulfatase deficiency mutationImportant
- rs137852850A;GCarrier of a multiple sulfatase deficiency mutationImportant
- rs137852851A;CCarrier of a multiple sulfatase deficiency mutationImportant
Source and license
Adapted from rs2819590 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.