Original source

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

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

Chromosome 4:110618669 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM961114

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 10230, 2010_April_001_057_PITX2_601542_0005

HGVS names

This variant has 23 HGVS names - Show

About this variant

This variant overlaps 15 transcripts and is associated with 3 phenotypes.

Variant displays