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rs773926353

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs773926353(C;G)
Make rs773926353(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position38467667
GeneRYR1
is asnp
is mentioned by
dbSNPrs773926353
ebirs773926353
HLIrs773926353
Exacrs773926353
Varsomers773926353
Maprs773926353
PheGenIrs773926353
hapmaprs773926353
1000 genomesrs773926353
hgdprs773926353
ensemblrs773926353
gopubmedrs773926353
geneviewrs773926353
scholarrs773926353
googlers773926353
pharmgkbrs773926353
gwascentralrs773926353
openSNPrs773926353
23andMers773926353
23andMe allrs773926353
SNP Nexus

SNPshotrs773926353
SNPdbers773926353
MSV3drs773926353
GWAS Ctlgrs773926353
Max Magnitude0
ClinVar
Risk rs773926353(G,T;G,T)
Alt rs773926353(G,T;G,T)
Reference rs773926353(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR1
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.38958307C>G
CLNSRC
CLNACC RCV000182604.1,