rs121908417
A SNP in the ACTN4 gene on chromosome 19. Its most notable genotype is C;T: Focal segmental glomerulosclerosis 1 (possible)
- Gene
- ACTN4
- Location
- Chr 1938,710,307 (GRCh38)
- Highest magnitude
- 3.5Important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;TMost notableBadFocal segmental glomerulosclerosis 1 (possible)
- T;TGoodcommon in clinvar
On SNPedia: (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
Focal segmental glomerulosclerosis Called i5900587 by 23andMe
C;T
Reported in some individuals to lead to focal segmental glomerulosclerosis 1. See OMIM entry linked to rs121908417.
Source and license
Adapted from rs121908417 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.