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rs768711283

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs768711283(A;A)
Make rs768711283(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position237770827
GeneRYR2
is asnp
is mentioned by
dbSNPrs768711283
ebirs768711283
HLIrs768711283
Exacrs768711283
Varsomers768711283
Maprs768711283
PheGenIrs768711283
hapmaprs768711283
1000 genomesrs768711283
hgdprs768711283
ensemblrs768711283
gopubmedrs768711283
geneviewrs768711283
scholarrs768711283
googlers768711283
pharmgkbrs768711283
gwascentralrs768711283
openSNPrs768711283
23andMers768711283
23andMe allrs768711283
SNP Nexus

SNPshotrs768711283
SNPdbers768711283
MSV3drs768711283
GWAS Ctlgrs768711283
Max Magnitude0
ClinVar
Risk rs768711283(A;A)
Alt rs768711283(A;A)
Reference rs768711283(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237934127G>A
CLNSRC
CLNACC RCV000182796.2,