Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S|MAF: 0.07 (C)
Location

Chromosome 1:110060421 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs60565963

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

Variant displays