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rs748937501

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs748937501(A;A)
Make rs748937501(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position237832627
GeneRYR2
is asnp
is mentioned by
dbSNPrs748937501
ebirs748937501
HLIrs748937501
Exacrs748937501
Varsomers748937501
Maprs748937501
PheGenIrs748937501
hapmaprs748937501
1000 genomesrs748937501
hgdprs748937501
ensemblrs748937501
gopubmedrs748937501
geneviewrs748937501
scholarrs748937501
googlers748937501
pharmgkbrs748937501
gwascentralrs748937501
openSNPrs748937501
23andMers748937501
23andMe allrs748937501
SNP Nexus

SNPshotrs748937501
SNPdbers748937501
MSV3drs748937501
GWAS Ctlgrs748937501
Max Magnitude0
ClinVar
Risk rs748937501(A;A)
Alt rs748937501(A;A)
Reference rs748937501(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237995927T>A
CLNSRC
CLNACC RCV000182855.2,