Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.33 (G)
Location

Chromosome 9:99150189 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR102176

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 6 transcripts, has 3901 sample genotypes and is mentioned in 16 citations.

Variant displays