Original source

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

A/T | Ancestral: T | Ambiguity code: W | MAF: 0.02 (T)

Chromosome 19:8978045 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_056594

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 1 transcript and has 2770 sample genotypes.

Variant displays