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rs1057517873

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517873(A;G)
Make rs1057517873(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position237832592
GeneRYR2
is asnp
is mentioned by
dbSNPrs1057517873
dbSNP (classic)rs1057517873
ClinGenrs1057517873
ebirs1057517873
HLIrs1057517873
Exacrs1057517873
Gnomadrs1057517873
Varsomers1057517873
LitVarrs1057517873
Maprs1057517873
PheGenIrs1057517873
Biobankrs1057517873
1000 genomesrs1057517873
hgdprs1057517873
ensemblrs1057517873
geneviewrs1057517873
scholarrs1057517873
googlers1057517873
pharmgkbrs1057517873
gwascentralrs1057517873
openSNPrs1057517873
23andMers1057517873
23andMe allrs1057517873
SNPshotrs1057517873
SNPdbers1057517873
MSV3drs1057517873
GWAS Ctlgrs1057517873
Max Magnitude0
ClinVar
Risk rs1057517873(G;G)
Alt rs1057517873(G;G)
Reference Rs1057517873(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237995892A>G
CLNSRC
CLNACC RCV000414217.1,