Original source

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

C/G | Ancestral: C | Ambiguity code: S | MAF: 0.12 (G)

Chromosome 16:109213 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs798609, rs57570743

This variation has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and has 1101 individual genotypes.

Variation displays