Original source

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

Synonyms

This variant has 4 synonyms - Show

HGVS names

This variant has 7 HGVS names - Show

About this variant

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

Variant displays