Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.10 (C)

Chromosome 12:11687466 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs364818, rs58265938

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 1376 individual genotypes.

Variation displays