Original source

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

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

Chromosome 4:73869807 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61661522

HGVS names

This variant has 3 HGVS names - Show

About this variant

Variant displays