Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

G/A/T | Ancestral: G | Ambiguity code: D | MAF: < 0.01 (T)

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


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 18 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 14 transcripts, has 2504 individual genotypes, is associated with 4 phenotypes and is mentioned in 3 citations.

Variation displays