Original source

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

G/A | Ancestral: G | Ambiguity code: R

Chromosome 3:8745788 (forward strand) | View in location tab


with COSMIC COSM94009 (G/A) ; HGMD-PUBLIC CM010790 ; PhenCode CAV3:c.377G>A (G/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

Variation displays