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rs758500988

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs758500988(A;A)
Make rs758500988(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position237832612
GeneRYR2
is asnp
is mentioned by
dbSNPrs758500988
ebirs758500988
HLIrs758500988
Exacrs758500988
Varsomers758500988
Maprs758500988
PheGenIrs758500988
hapmaprs758500988
1000 genomesrs758500988
hgdprs758500988
ensemblrs758500988
gopubmedrs758500988
geneviewrs758500988
scholarrs758500988
googlers758500988
pharmgkbrs758500988
gwascentralrs758500988
openSNPrs758500988
23andMers758500988
23andMe allrs758500988
SNP Nexus

SNPshotrs758500988
SNPdbers758500988
MSV3drs758500988
GWAS Ctlgrs758500988
Max Magnitude0
ClinVar
Risk rs758500988(A;A)
Alt rs758500988(A;A)
Reference rs758500988(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237995912T>A
CLNSRC
CLNACC RCV000182853.1,