Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 11:44267585 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM002931

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_008_ALX4_605420_0005, 13163

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

About this variant

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

Variation displays