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rs76335820

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs76335820(C;T)
Make rs76335820(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position29813701
GeneLOC100289283, PRRT2
is asnp
is mentioned by
dbSNPrs76335820
ebirs76335820
HLIrs76335820
Exacrs76335820
Varsomers76335820
Maprs76335820
PheGenIrs76335820
hapmaprs76335820
1000 genomesrs76335820
hgdprs76335820
ensemblrs76335820
gopubmedrs76335820
geneviewrs76335820
scholarrs76335820
googlers76335820
pharmgkbrs76335820
gwascentralrs76335820
openSNPrs76335820
23andMers76335820
23andMe allrs76335820
SNP Nexus

SNPshotrs76335820
SNPdbers76335820
MSV3drs76335820
GWAS Ctlgrs76335820
Max Magnitude0
ClinVar
Risk rs76335820(A,G,T;A,G,T)
Alt rs76335820(A,G,T;A,G,T)
Reference rs76335820(C;C)
Significance Other
Disease not specified Dystonia 10 not provided
Variation info
Gene LOC100289283 PRRT2
CLNDBN not specified Dystonia 10 not provided
Reversed 0
HGVS NC_000016.9:g.29825022C>A; NC_000016.9:g.29825022C>G; NC_000016.9:g.29825022C>T
CLNSRC ClinVar GeneReviews Emory University GeneDx University of Chicago
CLNACC RCV000188770.1, RCV000229187.1, RCV000055990.1, RCV000188771.2, RCV000082646.8, RCV000224146.1, RCV000233107.1,