Original source

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

Alleles
G/A/T|Ancestral: G|Ambiguity code: D
Location

Chromosome 19:1220488 (forward strand)|View in location tab

Co-located variants
Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 10855, Cosmic:25847

HGVS names

This variant has 26 HGVS names - Show

About this variant

This variant overlaps 20 transcripts, 1 regulatory feature and is associated with 3 phenotypes.

Variant displays