Original source

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

T/C/G | Ancestral: T | Ambiguity code: B

Chromosome 19:16482721 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_027945

HGVS names

This variant has 16 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 10 transcripts and has 268 sample genotypes.

Variant displays