Have questions? Visit https://www.reddit.com/r/SNPedia

rs267607005

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607005(A;G)
Make rs267607005(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position110812306
GeneRBM20
is asnp
is mentioned by
dbSNPrs267607005
ebirs267607005
HLIrs267607005
Exacrs267607005
Varsomers267607005
Maprs267607005
PheGenIrs267607005
hapmaprs267607005
1000 genomesrs267607005
hgdprs267607005
ensemblrs267607005
gopubmedrs267607005
geneviewrs267607005
scholarrs267607005
googlers267607005
pharmgkbrs267607005
gwascentralrs267607005
openSNPrs267607005
23andMers267607005
23andMe allrs267607005
SNP Nexus

SNPshotrs267607005
SNPdbers267607005
MSV3drs267607005
GWAS Ctlgrs267607005
Max Magnitude0
ClinVar
Risk rs267607005(G;G)
Alt rs267607005(G;G)
Reference rs267607005(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 1DD
Variation info
Gene RBM20
CLNDBN Dilated cardiomyopathy 1DD
Reversed 0
HGVS NC_000010.10:g.112572064A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000000296.2,