Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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