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rs764698152

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs764698152(C;T)
Make rs764698152(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position237445470
GeneRYR2
is asnp
is mentioned by
dbSNPrs764698152
ebirs764698152
HLIrs764698152
Exacrs764698152
Varsomers764698152
Maprs764698152
PheGenIrs764698152
hapmaprs764698152
1000 genomesrs764698152
hgdprs764698152
ensemblrs764698152
gopubmedrs764698152
geneviewrs764698152
scholarrs764698152
googlers764698152
pharmgkbrs764698152
gwascentralrs764698152
openSNPrs764698152
23andMers764698152
23andMe allrs764698152
SNP Nexus

SNPshotrs764698152
SNPdbers764698152
MSV3drs764698152
GWAS Ctlgrs764698152
Max Magnitude0
ClinVar
Risk rs764698152(T;T)
Alt rs764698152(T;T)
Reference rs764698152(C;C)
Significance Pathogenic
Disease not specified
Variation info
Gene RYR2
CLNDBN not specified
Reversed 0
HGVS NC_000001.10:g.237608770C>T
CLNSRC
CLNACC RCV000182678.2,