Original source

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

G/A/T | Ancestral: G | Ambiguity code: D | MAF: < 0.01 (T)

Chromosome 19:5831880 (forward strand) | View in location tab

Most severe consequence
Stop gained
Evidence status


This variant has 3 synonyms - Show

HGVS names

This variant has 22 HGVS names - Show

About this variant

This variant overlaps 24 transcripts, has 2810 sample genotypes and is mentioned in 4 citations.

Variant displays