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rs794729145

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794729145(C;C)
Make rs794729145(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position110797587
GeneRBM20
is asnp
is mentioned by
dbSNPrs794729145
ebirs794729145
HLIrs794729145
Exacrs794729145
Varsomers794729145
Maprs794729145
PheGenIrs794729145
hapmaprs794729145
1000 genomesrs794729145
hgdprs794729145
ensemblrs794729145
gopubmedrs794729145
geneviewrs794729145
scholarrs794729145
googlers794729145
pharmgkbrs794729145
gwascentralrs794729145
openSNPrs794729145
23andMers794729145
23andMe allrs794729145
SNP Nexus

SNPshotrs794729145
SNPdbers794729145
MSV3drs794729145
GWAS Ctlgrs794729145
Max Magnitude0
ClinVar
Risk rs794729145(C;C)
Alt rs794729145(C;C)
Reference rs794729145(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RBM20
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.112557345T>C
CLNSRC
CLNACC RCV000183853.2,