Original source

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

Alleles
A/- | Ancestral: A | MAF: 0.38 (-)
Location

Chromosome 12:21910318 (forward strand) | View in location tab

Most severe consequence
 
Splice region variant
Evidence status

Clinical significance

This variant has 4 synonyms - click the plus to show

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

About this variant

This variant overlaps 5 transcripts, has 2510 sample genotypes and is associated with 1 phenotype.

Variant displays