Original source

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

T/A | Ancestral: T | Ambiguity code: W | MAF: 0.22 (T)

Chromosome 3:8746799 (forward strand) | View in location tab


with PhenCode CAV3:c.*932T>A (T/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

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

About this variant

This variant overlaps 7 transcripts, has 1109 individual genotypes and is associated with 1 phenotype.

Variation displays