Original source

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

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

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

Co-located

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

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

This variant has 2 synonyms - click the plus to show

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

About this variant

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

Variant displays