Original source

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

Alleles
A/- | Ancestral: A
Location

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB ABCC9_4450-5delT_072111

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

About this variant

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

Variation displays