Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/G | Ancestral: C | Ambiguity code: S | MAF: 0.13 (G)

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs798609, rs57570743

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2508 sample genotypes.

Variant displays