Original source

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

Alleles
T/G|Ancestral: G|Ambiguity code: K|MAF: 0.05 (T)
Location

Chromosome 9:34126790 (forward strand)|View in location tab

Co-located variant

dbSNP rs113354924 (T/-)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59474536

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

Variant displays