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rs750259830

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs750259830(G;G)
Make rs750259830(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position237783789
GeneRYR2
is asnp
is mentioned by
dbSNPrs750259830
ebirs750259830
HLIrs750259830
Exacrs750259830
Varsomers750259830
Maprs750259830
PheGenIrs750259830
hapmaprs750259830
1000 genomesrs750259830
hgdprs750259830
ensemblrs750259830
gopubmedrs750259830
geneviewrs750259830
scholarrs750259830
googlers750259830
pharmgkbrs750259830
gwascentralrs750259830
openSNPrs750259830
23andMers750259830
23andMe allrs750259830
SNP Nexus

SNPshotrs750259830
SNPdbers750259830
MSV3drs750259830
GWAS Ctlgrs750259830
Max Magnitude0
ClinVar
Risk rs750259830(G;G)
Alt rs750259830(G;G)
Reference rs750259830(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237947089T>G
CLNSRC
CLNACC RCV000182807.1,