Have questions? Visit https://www.reddit.com/r/SNPedia

rs2819770

From SNPedia

Orientationminus
Stabilizedminus
Make rs2819770(A;A)
Make rs2819770(A;G)
Make rs2819770(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position237747704
GeneRYR2
is asnp
is mentioned by
dbSNPrs2819770
ebirs2819770
HLIrs2819770
Exacrs2819770
Varsomers2819770
Maprs2819770
PheGenIrs2819770
hapmaprs2819770
1000 genomesrs2819770
hgdprs2819770
ensemblrs2819770
gopubmedrs2819770
geneviewrs2819770
scholarrs2819770
googlers2819770
pharmgkbrs2819770
gwascentralrs2819770
openSNPrs2819770
23andMers2819770
23andMe allrs2819770
SNP Nexus

SNPshotrs2819770
SNPdbers2819770
MSV3drs2819770
GWAS Ctlgrs2819770
GMAF0.1524
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs2819770
PubMedID [PMID 17903301OA-icon.png]
Condition Exercise treadmill test traits
Gene RYR2
Risk Allele
pValue 4.00E-006
OR NA
95% CI



GET Evidence
rs2819770
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.18254
summary