Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M
Location

Chromosome 1:47417035 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM062745

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 2009_August_001_076_FOXE3_601094_0002, 9881

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