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rs113379223

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs113379223(A;A)
Make rs113379223(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position38460374
GeneRYR1
is asnp
is mentioned by
dbSNPrs113379223
dbSNP (old)rs113379223
ClinGenrs113379223
ebirs113379223
HLIrs113379223
Exacrs113379223
Gnomadrs113379223
Varsomers113379223
Maprs113379223
PheGenIrs113379223
Biobankrs113379223
1000 genomesrs113379223
hgdprs113379223
ensemblrs113379223
gopubmedrs113379223
geneviewrs113379223
scholarrs113379223
googlers113379223
pharmgkbrs113379223
gwascentralrs113379223
openSNPrs113379223
23andMers113379223
23andMe allrs113379223
SNPshotrs113379223
SNPdbers113379223
MSV3drs113379223
GWAS Ctlgrs113379223
Max Magnitude0
ClinVar
Risk rs113379223(A;A) rs113379223(C;C) rs113379223(T;T)
Alt rs113379223(A;A) rs113379223(C;C) rs113379223(T;T)
Reference Rs113379223(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR1
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.38951014G>C
CLNSRC
CLNACC RCV000478215.1,