Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

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

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

Co-located

with HGMD-PUBLIC CM980768

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 9868, 2010_April_001_050_FOXC1_601090_0002

This variation has 3 HGVS names - click the plus to show

Variation displays