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rs1064793256

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome1
Position237783714
GeneRYR2
is asnp
is mentioned by
dbSNPrs1064793256
dbSNP (old)rs1064793256
ClinGenrs1064793256
ebirs1064793256
HLIrs1064793256
Exacrs1064793256
Gnomadrs1064793256
Varsomers1064793256
LitVarrs1064793256
Maprs1064793256
PheGenIrs1064793256
Biobankrs1064793256
1000 genomesrs1064793256
hgdprs1064793256
ensemblrs1064793256
gopubmedrs1064793256
geneviewrs1064793256
scholarrs1064793256
googlers1064793256
pharmgkbrs1064793256
gwascentralrs1064793256
openSNPrs1064793256
23andMers1064793256
23andMe allrs1064793256
SNPshotrs1064793256
SNPdbers1064793256
MSV3drs1064793256
GWAS Ctlgrs1064793256
Max Magnitude0
ClinVar
Risk rs1064793256(G;G)
Alt rs1064793256(G;G)
Reference Rs1064793256(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237947014A>G
CLNSRC
CLNACC RCV000487006.1,