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rs118192153

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs118192153(C;T)
Make rs118192153(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position38585013
GeneRYR1
is asnp
is mentioned by
dbSNPrs118192153
ebirs118192153
HLIrs118192153
Exacrs118192153
Varsomers118192153
Maprs118192153
PheGenIrs118192153
hapmaprs118192153
1000 genomesrs118192153
hgdprs118192153
ensemblrs118192153
gopubmedrs118192153
geneviewrs118192153
scholarrs118192153
googlers118192153
pharmgkbrs118192153
gwascentralrs118192153
openSNPrs118192153
23andMers118192153
23andMe allrs118192153
SNP Nexus

SNPshotrs118192153
SNPdbers118192153
MSV3drs118192153
GWAS Ctlgrs118192153
Max Magnitude0
ClinVar
Risk rs118192153(G,T;G,T)
Alt rs118192153(G,T;G,T)
Reference rs118192153(C;C)
Significance Other
Disease not provided Central core disease
Variation info
Gene RYR1
CLNDBN not provided Central core disease
Reversed 0
HGVS NC_000019.9:g.39075653C>G; NC_000019.9:g.39075653C>T
CLNSRC ClinVar GeneReviews University of Washington
CLNACC RCV000173935.1, RCV000056173.3, RCV000119555.1,