Original source

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

A/- | Ancestral: A

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

Most severe consequence
Splice region variant
Evidence status

Clinical significance


LSDB ABCC9_4450-5delT_072111

HGVS names

This variant has 7 HGVS names - 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