Original source

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

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

Chromosome 11:44309645 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM010010

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_005_ALX4_605420_0001, 13159

This variation has 3 HGVS names - click the plus to show

About this variant

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

Variation displays