Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M
Location

Chromosome 11:6616696 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM003658

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 2 synonyms - Show

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 25 transcripts, is associated with 3 phenotypes and is mentioned in 2 citations.

Variant displays