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rs758785338

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs758785338(A;A)
Make rs758785338(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position237784010
GeneRYR2
is asnp
is mentioned by
dbSNPrs758785338
ebirs758785338
HLIrs758785338
Exacrs758785338
Varsomers758785338
Maprs758785338
PheGenIrs758785338
hapmaprs758785338
1000 genomesrs758785338
hgdprs758785338
ensemblrs758785338
gopubmedrs758785338
geneviewrs758785338
scholarrs758785338
googlers758785338
pharmgkbrs758785338
gwascentralrs758785338
openSNPrs758785338
23andMers758785338
23andMe allrs758785338
SNP Nexus

SNPshotrs758785338
SNPdbers758785338
MSV3drs758785338
GWAS Ctlgrs758785338
Max Magnitude0
ClinVar
Risk rs758785338(A;A)
Alt rs758785338(A;A)
Reference rs758785338(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237947310G>A
CLNSRC
CLNACC RCV000182814.2,