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 6:1610512 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM000158

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_053_FOXC1_601090_0005, 9871

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