Have questions? Visit https://www.reddit.com/r/SNPedia

rs397515576

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397515576(-;-)
Make rs397515576(-;T)
Make rs397515576(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position29813564
GeneLOC100289283, PRRT2
is asnp
is mentioned by
dbSNPrs397515576
ebirs397515576
HLIrs397515576
Exacrs397515576
Varsomers397515576
Maprs397515576
PheGenIrs397515576
hapmaprs397515576
1000 genomesrs397515576
hgdprs397515576
ensemblrs397515576
gopubmedrs397515576
geneviewrs397515576
scholarrs397515576
googlers397515576
pharmgkbrs397515576
gwascentralrs397515576
openSNPrs397515576
23andMers397515576
23andMe allrs397515576
SNP Nexus

SNPshotrs397515576
SNPdbers397515576
MSV3drs397515576
GWAS Ctlgrs397515576
Max Magnitude0
ClinVar
Risk rs397515576(T;T)
Alt rs397515576(T;T)
Reference rs397515576(;)
Significance Pathogenic
Disease Dystonia 10
Variation info
Gene LOC100289283 PRRT2
CLNDBN Dystonia 10
Reversed 0
HGVS NC_000016.9:g.29824885dupT
CLNSRC ClinVar GeneReviews
CLNACC RCV000055989.1,