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rs112563513

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs112563513(A;A)
Make rs112563513(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position38499223
GeneRYR1
is asnp
is mentioned by
dbSNPrs112563513
ebirs112563513
HLIrs112563513
Exacrs112563513
Varsomers112563513
Maprs112563513
PheGenIrs112563513
hapmaprs112563513
1000 genomesrs112563513
hgdprs112563513
ensemblrs112563513
gopubmedrs112563513
geneviewrs112563513
scholarrs112563513
googlers112563513
pharmgkbrs112563513
gwascentralrs112563513
openSNPrs112563513
23andMers112563513
23andMe allrs112563513
SNP Nexus

SNPshotrs112563513
SNPdbers112563513
MSV3drs112563513
GWAS Ctlgrs112563513
Max Magnitude0
ClinVar
Risk rs112563513(A;A)
Alt rs112563513(A;A)
Reference rs112563513(G;G)
Significance Untested
Disease not provided
Variation info
Gene RYR1
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.38989863G>A
CLNSRC
CLNACC RCV000119673.1,