Original source

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

C/G | Ancestral: G | Ambiguity code: S | MAF: 0.36 (G)

Chromosome 4:94884091 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs61007456

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 3120 sample genotypes.

Variant displays