Original source

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

Alleles
G/A/T|Ancestral: G|Ambiguity code: D
Location

Chromosome 11:44275505 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM060200

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 13164, 2010_April_001_009_ALX4_605420_0006

HGVS names

This variant has 6 HGVS names - Show

About this variant

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

Variant displays