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rs794729148

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729148(C;T)
Make rs794729148(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position110810449
GeneRBM20
is asnp
is mentioned by
dbSNPrs794729148
ebirs794729148
HLIrs794729148
Exacrs794729148
Varsomers794729148
Maprs794729148
PheGenIrs794729148
hapmaprs794729148
1000 genomesrs794729148
hgdprs794729148
ensemblrs794729148
gopubmedrs794729148
geneviewrs794729148
scholarrs794729148
googlers794729148
pharmgkbrs794729148
gwascentralrs794729148
openSNPrs794729148
23andMers794729148
23andMe allrs794729148
SNP Nexus

SNPshotrs794729148
SNPdbers794729148
MSV3drs794729148
GWAS Ctlgrs794729148
Max Magnitude0
ClinVar
Risk rs794729148(T;T)
Alt rs794729148(T;T)
Reference rs794729148(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RBM20
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.112570207C>T
CLNSRC
CLNACC RCV000183858.1,