Original source

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

Alleles
G/A/C|Ancestral: C|Ambiguity code: V|MAF: 0.16 (C)
Location

Chromosome 6:52419923 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs3761989

HGVS names

This variant has 2 HGVS names - Show

About this variant

Variant displays