Original source

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

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

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

Co-located

with HGMD-PUBLIC CM030828

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 9566, 2010_April_001_033_CSRP3_600824_0002

This variant has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and is associated with 2 phenotypes.

Variant displays