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rs794729143

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729143(C;T)
Make rs794729143(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position110781765
GeneRBM20
is asnp
is mentioned by
dbSNPrs794729143
ebirs794729143
HLIrs794729143
Exacrs794729143
Varsomers794729143
Maprs794729143
PheGenIrs794729143
hapmaprs794729143
1000 genomesrs794729143
hgdprs794729143
ensemblrs794729143
gopubmedrs794729143
geneviewrs794729143
scholarrs794729143
googlers794729143
pharmgkbrs794729143
gwascentralrs794729143
openSNPrs794729143
23andMers794729143
23andMe allrs794729143
SNP Nexus

SNPshotrs794729143
SNPdbers794729143
MSV3drs794729143
GWAS Ctlgrs794729143
Max Magnitude0
ClinVar
Risk rs794729143(T;T)
Alt rs794729143(T;T)
Reference rs794729143(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene RBM20
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.112541523C>T
CLNSRC
CLNACC RCV000183849.1,