Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.06 (C)
Location

Chromosome 3:8787189 (forward strand) | View in location tab

Co-located

with PhenCode CAV3:c.115-23G>C (G/C)

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

Variation displays