Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: 0.21 (T)
Location

Chromosome 3:38773939 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17360491, rs59649921

HGVS names

This variant has 2 HGVS names - Show

About this variant

Variant displays