Original source

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

Alleles
T/A/C|Ancestral: T|Ambiguity code: H
Location

Chromosome 6:1610780 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CD117364, CM980766

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_052_FOXC1_601090_0004, 9870

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature and is associated with 4 phenotypes.

Variant displays