Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 6:1610690 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM980764

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_054_FOXC1_601090_0008, 9874

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

Variation displays