Original source

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

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

Chromosome 11:19188245 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM030828

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_033_CSRP3_600824_0002, 9566

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 3 transcripts, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays