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rs794729149

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729149(A;A)
Make rs794729149(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position110812307
GeneRBM20
is asnp
is mentioned by
dbSNPrs794729149
ebirs794729149
HLIrs794729149
Exacrs794729149
Varsomers794729149
Maprs794729149
PheGenIrs794729149
hapmaprs794729149
1000 genomesrs794729149
hgdprs794729149
ensemblrs794729149
gopubmedrs794729149
geneviewrs794729149
scholarrs794729149
googlers794729149
pharmgkbrs794729149
gwascentralrs794729149
openSNPrs794729149
23andMers794729149
23andMe allrs794729149
SNP Nexus

SNPshotrs794729149
SNPdbers794729149
MSV3drs794729149
GWAS Ctlgrs794729149
Max Magnitude0
ClinVar
Risk rs794729149(A;A)
Alt rs794729149(A;A)
Reference rs794729149(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RBM20
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.112572065G>A
CLNSRC
CLNACC RCV000183863.2,