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rs267607001

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607001(A;A)
Make rs267607001(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position110812298
GeneRBM20
is asnp
is mentioned by
dbSNPrs267607001
ebirs267607001
HLIrs267607001
Exacrs267607001
Varsomers267607001
Maprs267607001
PheGenIrs267607001
hapmaprs267607001
1000 genomesrs267607001
hgdprs267607001
ensemblrs267607001
gopubmedrs267607001
geneviewrs267607001
scholarrs267607001
googlers267607001
pharmgkbrs267607001
gwascentralrs267607001
openSNPrs267607001
23andMers267607001
23andMe allrs267607001
SNP Nexus

SNPshotrs267607001
SNPdbers267607001
MSV3drs267607001
GWAS Ctlgrs267607001
Max Magnitude0
ClinVar
Risk rs267607001(A;A)
Alt rs267607001(A;A)
Reference rs267607001(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 1DD not provided
Variation info
Gene RBM20
CLNDBN Dilated cardiomyopathy 1DD not provided
Reversed 0
HGVS NC_000010.10:g.112572056G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000293.4, RCV000183859.2,