Original source

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

Alleles
C/A/T|Ancestral: C|Ambiguity code: H
Location

Chromosome 16:20348994 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM023182

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 38 HGVS names - Show

About this variant

This variant overlaps 24 transcripts and is associated with 3 phenotypes.

Variant displays