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rs267607002

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607002(A;A)
Make rs267607002(A;C)
ReferenceGRCh38 38.1/141
Chromosome10
Position110812303
GeneRBM20
is asnp
is mentioned by
dbSNPrs267607002
ebirs267607002
HLIrs267607002
Exacrs267607002
Varsomers267607002
Maprs267607002
PheGenIrs267607002
hapmaprs267607002
1000 genomesrs267607002
hgdprs267607002
ensemblrs267607002
gopubmedrs267607002
geneviewrs267607002
scholarrs267607002
googlers267607002
pharmgkbrs267607002
gwascentralrs267607002
openSNPrs267607002
23andMers267607002
23andMe allrs267607002
SNP Nexus

SNPshotrs267607002
SNPdbers267607002
MSV3drs267607002
GWAS Ctlgrs267607002
Max Magnitude0
ClinVar
Risk rs267607002(A,T;A,T)
Alt rs267607002(A,T;A,T)
Reference rs267607002(C;C)
Significance Other
Disease Dilated cardiomyopathy 1DD not provided Primary dilated cardiomyopathy not specified
Variation info
Gene RBM20
CLNDBN Dilated cardiomyopathy 1DD not provided Primary dilated cardiomyopathy not specified
Reversed 0
HGVS NC_000010.10:g.112572061C>A; NC_000010.10:g.112572061C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000294.4, RCV000183860.2, RCV000208477.1, RCV000036953.2, RCV000170520.3, RCV000225732.2,