Original source

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

Alleles
C/A | Ambiguity code: M
Location

Chromosome 3:8746804 (forward strand) | View in location tab

Co-located

with PhenCode CAV3:c.*937C>A (C/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB CAV3_25

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

Variation displays