Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y
Location

Chromosome 6:1610837 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM980768, CM117355, CM117352

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 9868, 2010_April_001_050_FOXC1_601090_0002

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays