This variant has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
C/A/G/T|Ancestral: C|Ambiguity code: N
Location

Chromosome 6:1610823 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM980767

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_051_FOXC1_601090_0003, 9869

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays