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rs771994461

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs771994461(C;T)
Make rs771994461(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position237784084
GeneRYR2
is asnp
is mentioned by
dbSNPrs771994461
ebirs771994461
HLIrs771994461
Exacrs771994461
Varsomers771994461
Maprs771994461
PheGenIrs771994461
hapmaprs771994461
1000 genomesrs771994461
hgdprs771994461
ensemblrs771994461
gopubmedrs771994461
geneviewrs771994461
scholarrs771994461
googlers771994461
pharmgkbrs771994461
gwascentralrs771994461
openSNPrs771994461
23andMers771994461
23andMe allrs771994461
SNP Nexus

SNPshotrs771994461
SNPdbers771994461
MSV3drs771994461
GWAS Ctlgrs771994461
Max Magnitude0
ClinVar
Risk rs771994461(T;T)
Alt rs771994461(T;T)
Reference rs771994461(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237947384C>A
CLNSRC
CLNACC RCV000182816.1,