Original source

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

Alleles
T/G|Ancestral: G|Ambiguity code: K|MAF: < 0.01 (T)
Location

Chromosome 15:67178697 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60640041

HGVS names

This variant has 9 HGVS names - Show

About this variant

Variant displays