Original source

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

G/C | Ancestral: G | Ambiguity code: S | MAF: 0.41 (C)

Chromosome 16:3144656 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs513974

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2777 sample genotypes.

Variant displays