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rs748194372

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs748194372(A;A)
Make rs748194372(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position237702017
GeneRYR2
is asnp
is mentioned by
dbSNPrs748194372
ebirs748194372
HLIrs748194372
Exacrs748194372
Varsomers748194372
Maprs748194372
PheGenIrs748194372
hapmaprs748194372
1000 genomesrs748194372
hgdprs748194372
ensemblrs748194372
gopubmedrs748194372
geneviewrs748194372
scholarrs748194372
googlers748194372
pharmgkbrs748194372
gwascentralrs748194372
openSNPrs748194372
23andMers748194372
23andMe allrs748194372
SNP Nexus

SNPshotrs748194372
SNPdbers748194372
MSV3drs748194372
GWAS Ctlgrs748194372
Max Magnitude0
ClinVar
Risk rs748194372(A;A)
Alt rs748194372(A;A)
Reference rs748194372(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237865317G>A
CLNSRC
CLNACC RCV000171172.1,