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rs727505310

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727505310(C;T)
Make rs727505310(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position110812355
GeneRBM20
is asnp
is mentioned by
dbSNPrs727505310
ebirs727505310
HLIrs727505310
Exacrs727505310
Varsomers727505310
Maprs727505310
PheGenIrs727505310
hapmaprs727505310
1000 genomesrs727505310
hgdprs727505310
ensemblrs727505310
gopubmedrs727505310
geneviewrs727505310
scholarrs727505310
googlers727505310
pharmgkbrs727505310
gwascentralrs727505310
openSNPrs727505310
23andMers727505310
23andMe allrs727505310
SNP Nexus

SNPshotrs727505310
SNPdbers727505310
MSV3drs727505310
GWAS Ctlgrs727505310
Max Magnitude0
ClinVar
Risk rs727505310(T;T)
Alt rs727505310(T;T)
Reference rs727505310(C;C)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene RBM20
CLNDBN not specified not provided
Reversed 0
HGVS NC_000010.10:g.112572113C>T
CLNSRC
CLNACC RCV000156848.2, RCV000183867.1,