Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.16 (T)
Location

Chromosome 1:12203862 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs9430686, rs17881572

HGVS names

This variant has 3 HGVS names - Show

About this variant

Variant displays