Original source

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

Alleles
G/A/C|Ancestral: T|Ambiguity code: V|MAF: 0.02 (C)
Location

Chromosome 9:136673673 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

Variant displays