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rs727503396

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503396(A;A)
Make rs727503396(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position237369589
GeneRYR2
is asnp
is mentioned by
dbSNPrs727503396
ebirs727503396
HLIrs727503396
Exacrs727503396
Varsomers727503396
Maprs727503396
PheGenIrs727503396
hapmaprs727503396
1000 genomesrs727503396
hgdprs727503396
ensemblrs727503396
gopubmedrs727503396
geneviewrs727503396
scholarrs727503396
googlers727503396
pharmgkbrs727503396
gwascentralrs727503396
openSNPrs727503396
23andMers727503396
23andMe allrs727503396
SNP Nexus

SNPshotrs727503396
SNPdbers727503396
MSV3drs727503396
GWAS Ctlgrs727503396
Max Magnitude0
ClinVar
Risk rs727503396(A;A)
Alt rs727503396(A;A)
Reference rs727503396(G;G)
Significance Probable-Pathogenic
Disease not specified Ventricular tachycardia
Variation info
Gene RYR2
CLNDBN not specified Ventricular tachycardia, catecholaminergic polymorphic, 1
Reversed 0
HGVS NC_000001.10:g.237532889G>A
CLNSRC
CLNACC RCV000151753.1, RCV000157442.1,