Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S|MAF: 0.13 (C)
Location

Chromosome 9:136682074 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17251783

HGVS names

This variant has 5 HGVS names - Show

About this variant

Variant displays