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rs113928116

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs113928116(C;C)
Make rs113928116(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position38536071
GeneRYR1
is asnp
is mentioned by
dbSNPrs113928116
dbSNP (classic)rs113928116
ClinGenrs113928116
ebirs113928116
HLIrs113928116
Exacrs113928116
Gnomadrs113928116
Varsomers113928116
LitVarrs113928116
Maprs113928116
PheGenIrs113928116
Biobankrs113928116
1000 genomesrs113928116
hgdprs113928116
ensemblrs113928116
geneviewrs113928116
scholarrs113928116
googlers113928116
pharmgkbrs113928116
gwascentralrs113928116
openSNPrs113928116
23andMers113928116
23andMe allrs113928116
SNPshotrs113928116
SNPdbers113928116
MSV3drs113928116
GWAS Ctlgrs113928116
Max Magnitude0
ClinVar
Risk rs113928116(C;C) rs113928116(T;T)
Alt rs113928116(C;C) rs113928116(T;T)
Reference Rs113928116(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR1
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.39026711G>T
CLNSRC
CLNACC RCV000438320.1,