Original source

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

G/A/T | Ancestral: G | Ambiguity code: D

Chromosome 7:55173083 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_019296

HGVS names

This variant has 22 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 14 transcripts, has 829 sample genotypes and is mentioned in 1 citation.

Variant displays