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rs137852603

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852603(A;C)
Make rs137852603(C;C)
ReferenceGRCh38 38.1/141
Chromosome10
Position110280017
GeneMXI1
is asnp
is mentioned by
dbSNPrs137852603
ebirs137852603
HLIrs137852603
Exacrs137852603
Varsomers137852603
Maprs137852603
PheGenIrs137852603
hapmaprs137852603
1000 genomesrs137852603
hgdprs137852603
ensemblrs137852603
gopubmedrs137852603
geneviewrs137852603
scholarrs137852603
googlers137852603
pharmgkbrs137852603
gwascentralrs137852603
openSNPrs137852603
23andMers137852603
23andMe allrs137852603
SNP Nexus

SNPshotrs137852603
SNPdbers137852603
MSV3drs137852603
GWAS Ctlgrs137852603
Max Magnitude0
OMIM600020
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137852603(C;C)
Alt rs137852603(C;C)
Reference rs137852603(A;A)
Significance Pathogenic
Disease Malignant tumor of prostate
Variation info
Gene MXI1
CLNDBN Malignant tumor of prostate
Reversed 0
HGVS NC_000010.10:g.112039775A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010144.4,