Original source

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

T/A/C | Ancestral: T | Ambiguity code: H | MAF: 0.22 (C)

Chromosome 19:8954956 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


This variant has 5 synonyms - Show

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 13 chips - Show

About this variant

This variant overlaps 2 transcripts and has 3649 sample genotypes.

Variant displays