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rs387906417

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906417(C;C)
Make rs387906417(C;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position110279296
GeneMXI1
is asnp
is mentioned by
dbSNPrs387906417
ebirs387906417
HLIrs387906417
Exacrs387906417
Varsomers387906417
Maprs387906417
PheGenIrs387906417
hapmaprs387906417
1000 genomesrs387906417
hgdprs387906417
ensemblrs387906417
gopubmedrs387906417
geneviewrs387906417
scholarrs387906417
googlers387906417
pharmgkbrs387906417
gwascentralrs387906417
openSNPrs387906417
23andMers387906417
23andMe allrs387906417
SNP Nexus

SNPshotrs387906417
SNPdbers387906417
MSV3drs387906417
GWAS Ctlgrs387906417
Max Magnitude0
ClinVar
Risk rs387906417(C;C)
Alt rs387906417(C;C)
Reference rs387906417(T;T)
Significance Pathogenic
Disease Malignant tumor of prostate
Variation info
Gene MXI1
CLNDBN Malignant tumor of prostate
Reversed 0
HGVS NC_000010.10:g.112039054T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010143.2,