Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.34 (A)

Chromosome 17:43044391 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 11 transcripts, has 3844 sample genotypes, is associated with 1 phenotype and is mentioned in 6 citations.

Variant displays