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rs794729144

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729144(C;T)
Make rs794729144(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position110781792
GeneRBM20
is asnp
is mentioned by
dbSNPrs794729144
ebirs794729144
HLIrs794729144
Exacrs794729144
Varsomers794729144
Maprs794729144
PheGenIrs794729144
hapmaprs794729144
1000 genomesrs794729144
hgdprs794729144
ensemblrs794729144
gopubmedrs794729144
geneviewrs794729144
scholarrs794729144
googlers794729144
pharmgkbrs794729144
gwascentralrs794729144
openSNPrs794729144
23andMers794729144
23andMe allrs794729144
SNP Nexus

SNPshotrs794729144
SNPdbers794729144
MSV3drs794729144
GWAS Ctlgrs794729144
Max Magnitude0
ClinVar
Risk rs794729144(T;T)
Alt rs794729144(T;T)
Reference rs794729144(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene RBM20
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.112541550C>T
CLNSRC
CLNACC RCV000183850.2,