Original source

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

Alleles
A/- | Ancestral: A
Location

Chromosome 12:21806065 (forward strand) | View in location tab

Co-located

with ClinVar rs730880348 (-/A)

Most severe consequence
 
Splice region variant
Evidence status

Clinical significance

Synonyms

LSDB ABCC9_4450-5delT_072111

This variant has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts, has 1 sample genotype, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays