Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome 11:44275389 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM010012

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 13160, 2010_April_001_006_ALX4_605420_0002

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 1 transcript and is associated with 2 phenotypes.

Variant displays