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rs727504859

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504859(A;A)
Make rs727504859(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position110821365
GeneRBM20
is asnp
is mentioned by
dbSNPrs727504859
ebirs727504859
HLIrs727504859
Exacrs727504859
Varsomers727504859
Maprs727504859
PheGenIrs727504859
hapmaprs727504859
1000 genomesrs727504859
hgdprs727504859
ensemblrs727504859
gopubmedrs727504859
geneviewrs727504859
scholarrs727504859
googlers727504859
pharmgkbrs727504859
gwascentralrs727504859
openSNPrs727504859
23andMers727504859
23andMe allrs727504859
SNP Nexus

SNPshotrs727504859
SNPdbers727504859
MSV3drs727504859
GWAS Ctlgrs727504859
Max Magnitude0
ClinVar
Risk rs727504859(A;A)
Alt rs727504859(A;A)
Reference rs727504859(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene RBM20
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000010.10:g.112581123G>A
CLNSRC
CLNACC RCV000156214.1,