Original source

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

Alleles
C/G|Ancestral: T|Ambiguity code: S|MAF: 0.26 (C)
Location

Chromosome 13:28067433 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57898425

HGVS names

This variant has 5 HGVS names - Show

About this variant

Variant displays