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 17:28405360 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 5 synonyms - Show

HGVS names

This variant has 30 HGVS names - Show

About this variant

This variant overlaps 24 transcripts, 1 regulatory feature, is associated with 7 phenotypes and is mentioned in 3 citations.

Variant displays