Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D
Location

Chromosome 3:8745688 (forward strand) | View in location tab

Co-located

with COSMIC COSM2828095 (G/A) ; HGMD-PUBLIC CM030812 ; PhenCode CAV3:c.277G>A (G/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

This variation has 16 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays