Original source

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

Alleles
T/A|Ancestral: T|Ambiguity code: W
Location

Chromosome 22:19763273 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM033031

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 7 transcripts, is associated with 4 phenotypes and is mentioned in 1 citation.

Variant displays