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rs753850982

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs753850982(A;A)
Make rs753850982(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position237783995
GeneRYR2
is asnp
is mentioned by
dbSNPrs753850982
ebirs753850982
HLIrs753850982
Exacrs753850982
Varsomers753850982
Maprs753850982
PheGenIrs753850982
hapmaprs753850982
1000 genomesrs753850982
hgdprs753850982
ensemblrs753850982
gopubmedrs753850982
geneviewrs753850982
scholarrs753850982
googlers753850982
pharmgkbrs753850982
gwascentralrs753850982
openSNPrs753850982
23andMers753850982
23andMe allrs753850982
SNP Nexus

SNPshotrs753850982
SNPdbers753850982
MSV3drs753850982
GWAS Ctlgrs753850982
Max Magnitude0
ClinVar
Risk rs753850982(A;A)
Alt rs753850982(A;A)
Reference rs753850982(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237947295G>A
CLNSRC
CLNACC RCV000182812.2,