Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 5 synonyms - click the plus to show

This variant has 30 HGVS names - click the plus to 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