Original source

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

G/T | Ambiguity code: K | MAF: < 0.01 (T)

Chromosome 19:8939435 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


This variant has 2 synonyms - Show

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 1 transcript and has 2770 sample genotypes.

Variant displays