Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

with dbSNP rs113354924 (T/-)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59474536

This variant has 2 HGVS names - click the plus to show

This variant has assays on 4 chips - click the plus to show

About this variant

Variant displays