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rs533330664

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs533330664(C;T)
Make rs533330664(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position237550628
GeneRYR2
is asnp
is mentioned by
dbSNPrs533330664
ebirs533330664
HLIrs533330664
Exacrs533330664
Varsomers533330664
Maprs533330664
PheGenIrs533330664
hapmaprs533330664
1000 genomesrs533330664
hgdprs533330664
ensemblrs533330664
gopubmedrs533330664
geneviewrs533330664
scholarrs533330664
googlers533330664
pharmgkbrs533330664
gwascentralrs533330664
openSNPrs533330664
23andMers533330664
23andMe allrs533330664
SNP Nexus

SNPshotrs533330664
SNPdbers533330664
MSV3drs533330664
GWAS Ctlgrs533330664
Max Magnitude0
ClinVar
Risk rs533330664(T;T)
Alt rs533330664(T;T)
Reference rs533330664(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237713928C>T
CLNSRC
CLNACC RCV000182708.2,