rs770241913
A SNP in the SUMF1 gene on chromosome 3. Its most notable genotype is -;C: Carrier of a multiple sulfatase deficiency mutation
- Gene
- SUMF1
- Location
- Chr 34,418,074 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- -;CMost notableBadCarrier of a multiple sulfatase deficiency mutation
- C;CGoodcommon in clinvar
On SNPedia: (-;C), (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
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
Notes
From SNPedia
Notes
-;C
Unaffected in absence of a second SUMF1 gene mutation; see links to that gene via main rs-page.
Source and license
Adapted from rs770241913 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.