Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: < 0.01 (C)
Location

Chromosome 12:32878903 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

Synonyms

LSDB PKP2_336+17T_G_112410

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays