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rs267607003

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607003(C;T)
Make rs267607003(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position110812310
GeneRBM20
is asnp
is mentioned by
dbSNPrs267607003
ebirs267607003
HLIrs267607003
Exacrs267607003
Varsomers267607003
Maprs267607003
PheGenIrs267607003
hapmaprs267607003
1000 genomesrs267607003
hgdprs267607003
ensemblrs267607003
gopubmedrs267607003
geneviewrs267607003
scholarrs267607003
googlers267607003
pharmgkbrs267607003
gwascentralrs267607003
openSNPrs267607003
23andMers267607003
23andMe allrs267607003
SNP Nexus

SNPshotrs267607003
SNPdbers267607003
MSV3drs267607003
GWAS Ctlgrs267607003
Max Magnitude0
ClinVar
Risk rs267607003(T;T)
Alt rs267607003(T;T)
Reference rs267607003(C;C)
Significance Pathogenic
Disease not provided Dilated cardiomyopathy 1DD Primary dilated cardiomyopathy
Variation info
Gene RBM20
CLNDBN not provided Dilated cardiomyopathy 1DD Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000010.10:g.112572068C>G; NC_000010.10:g.112572068C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000183864.2, RCV000000292.4, RCV000183865.2, RCV000211851.1,