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rs786205454

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205454(A;A)
Make rs786205454(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237387363
GeneRYR2
is asnp
is mentioned by
dbSNPrs786205454
ebirs786205454
HLIrs786205454
Exacrs786205454
Varsomers786205454
Maprs786205454
PheGenIrs786205454
hapmaprs786205454
1000 genomesrs786205454
hgdprs786205454
ensemblrs786205454
gopubmedrs786205454
geneviewrs786205454
scholarrs786205454
googlers786205454
pharmgkbrs786205454
gwascentralrs786205454
openSNPrs786205454
23andMers786205454
23andMe allrs786205454
SNP Nexus

SNPshotrs786205454
SNPdbers786205454
MSV3drs786205454
GWAS Ctlgrs786205454
Max Magnitude0
ClinVar
Risk rs786205454(A;A)
Alt rs786205454(A;A)
Reference rs786205454(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237550663G>A
CLNSRC
CLNACC RCV000171171.1,