rs876657646
A SNP in the FLCN gene on chromosome 17. Its most notable genotype is A;G: Birt-Hogg-Dube Syndrome
- Gene
- FLCN
- Location
- Chr 1717,223,987 (GRCh38)
- Highest magnitude
- 5.0Very important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- A;GMost notableBadBirt-Hogg-Dube Syndrome
- A;AGoodcommon in clinvar
SNPedia records rs876657646 on the minus strand: (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other FLCN SNPs
- rs80338682-;GBirt-Hogg-Dube SyndromeVery important
- rs80338683-;GBirt-Hogg-Dube syndromeVery important
- rs137852929G;TBirt-Hogg-Dube SyndromeVery important
- rs368778627C;TBirt-Hogg-Dube SyndromeVery important
- rs398124524A;GBirt-Hogg-Dube SyndromeVery important
- rs398124525-;GBirt-Hogg-Dube SyndromeVery important
- rs398124526-;GBirt-Hogg-Dube SyndromeVery important
- rs398124527-;ABirt-Hogg-Dube SyndromeVery important
Source and license
Adapted from rs876657646 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.