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rs730882066

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730882066(-;-)
Make rs730882066(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position29814425
GenePAGR1, PRRT2
is asnp
is mentioned by
dbSNPrs730882066
ebirs730882066
HLIrs730882066
Exacrs730882066
Varsomers730882066
Maprs730882066
PheGenIrs730882066
hapmaprs730882066
1000 genomesrs730882066
hgdprs730882066
ensemblrs730882066
gopubmedrs730882066
geneviewrs730882066
scholarrs730882066
googlers730882066
pharmgkbrs730882066
gwascentralrs730882066
openSNPrs730882066
23andMers730882066
23andMe allrs730882066
SNP Nexus

SNPshotrs730882066
SNPdbers730882066
MSV3drs730882066
GWAS Ctlgrs730882066
Max Magnitude0
ClinVar
Risk rs730882066(;)
Alt rs730882066(;)
Reference rs730882066(A;A)
Significance Pathogenic
Disease Dystonia 10
Variation info
Gene PAGR1 PRRT2
CLNDBN Dystonia 10
Reversed 0
HGVS NC_000016.9:g.29825746delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000024168.4,