Original source

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

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

Chromosome 6:1610706 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM980765

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_055_FOXC1_601090_0009, 9875

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

Variation displays