Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

T/A|Ancestral: T|Ambiguity code: W|MAF: 0.16 (T)

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

Co-located variant

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

Most severe consequence
Intron variant
Evidence status

Clinical significance


This variant has 2 synonyms - Show

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 7 transcripts, has 2511 sample genotypes and is associated with 1 phenotype.

Variant displays