Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 2 HGVS names - click the plus to show

About this variant

Variant displays