Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: < 0.01 (A)
Location

Chromosome 11:112086941 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM003169

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 22 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 24 transcripts, 1 regulatory feature, has 2505 sample genotypes and is associated with 8 phenotypes.

Variant displays