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rs10500279

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs10500279(C;C)
Make rs10500279(C;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position38544428
GeneRYR1
is asnp
is mentioned by
dbSNPrs10500279
ebirs10500279
HLIrs10500279
Exacrs10500279
Varsomers10500279
Maprs10500279
PheGenIrs10500279
hapmaprs10500279
1000 genomesrs10500279
hgdprs10500279
ensemblrs10500279
gopubmedrs10500279
geneviewrs10500279
scholarrs10500279
googlers10500279
pharmgkbrs10500279
gwascentralrs10500279
openSNPrs10500279
23andMers10500279
23andMe allrs10500279
SNP Nexus

SNPshotrs10500279
SNPdbers10500279
MSV3drs10500279
GWAS Ctlgrs10500279
GMAF0.07759
Max Magnitude0
? (C;C) (C;G) (G;G) 28

[PMID 21828061] Common variants in RYR1 are associated with left ventricular hypertrophy assessed by electrocardiogram