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rs1085307997

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome1
Position237781598
GeneRYR2
is asnp
is mentioned by
dbSNPrs1085307997
dbSNP (old)rs1085307997
ClinGenrs1085307997
ebirs1085307997
HLIrs1085307997
Exacrs1085307997
Gnomadrs1085307997
Varsomers1085307997
Maprs1085307997
PheGenIrs1085307997
Biobankrs1085307997
1000 genomesrs1085307997
hgdprs1085307997
ensemblrs1085307997
gopubmedrs1085307997
geneviewrs1085307997
scholarrs1085307997
googlers1085307997
pharmgkbrs1085307997
gwascentralrs1085307997
openSNPrs1085307997
23andMers1085307997
23andMe allrs1085307997
SNPshotrs1085307997
SNPdbers1085307997
MSV3drs1085307997
GWAS Ctlgrs1085307997
Max Magnitude0
ClinVar
Risk rs1085307997(G;G)
Alt rs1085307997(G;G)
Reference Rs1085307997(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237944898A>G
CLNSRC
CLNACC RCV000490203.1,