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rs790889

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs790889(C;C)
Make rs790889(C;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position237783664
GeneRYR2
is asnp
is mentioned by
dbSNPrs790889
ebirs790889
HLIrs790889
Exacrs790889
Varsomers790889
Maprs790889
PheGenIrs790889
hapmaprs790889
1000 genomesrs790889
hgdprs790889
ensemblrs790889
gopubmedrs790889
geneviewrs790889
scholarrs790889
googlers790889
pharmgkbrs790889
gwascentralrs790889
openSNPrs790889
23andMers790889
23andMe allrs790889
SNP Nexus

SNPshotrs790889
SNPdbers790889
MSV3drs790889
GWAS Ctlgrs790889
Max Magnitude0

[PMID 24978818OA-icon.png] RYR2 sequencing reveals novel missense mutations in a Kazakh idiopathic ventricular tachycardia study cohort.


ClinVar
Risk rs790889(C;C)
Alt rs790889(C;C)
Reference rs790889(T;T)
Significance Non-pathogenic
Disease not specified
Variation info
Gene RYR2
CLNDBN not specified
Reversed 0
HGVS NC_000001.10:g.237946964T>C
CLNSRC ClinVar
CLNACC RCV000036668.3,