Original source

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

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

Chromosome 7:55143357 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_019293

HGVS names

This variant has 40 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 18 transcripts, has 833 sample genotypes and is mentioned in 1 citation.

Variant displays