Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: 0.33 (T)
Location

Chromosome 3:50254761 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58074030

HGVS names

This variant has 11 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

Variant displays