rs397515785
A SNP in the LOC105370809 gene on chromosome 15. Its most notable genotype is -;TGGGATTTACC: Marfan syndrome mutation
- Gene
- LOC105370809
- Location
- Chr 1548,644,730 (GRCh38)
- Highest magnitude
- 5.5Very important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- -;TGGGATTTACCMost notableBadMarfan syndrome mutation
- CCTGGGATTTA;CCTGGGATTTAGoodcommon/normal
- CTGGGATTTAC;CTGGGATTTACGoodcommon in clinvar
- I;IGoodcommon genotype
- TGGGATTTACC;TGGGATTTACCGoodcommon in clinvar
On SNPedia: (-;TGGGATTTACC), (CCTGGGATTTA;CCTGGGATTTA), (CTGGGATTTAC;CTGGGATTTAC), (I;I), (TGGGATTTACC;TGGGATTTACC). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Notes
From SNPedia
Notes
-;TGGGATTTACC
See links via main rs-page
Source and license
Adapted from rs397515785 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.