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rs137852604

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852604(C;T)
Make rs137852604(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position110228276
GeneMXI1
is asnp
is mentioned by
dbSNPrs137852604
ebirs137852604
HLIrs137852604
Exacrs137852604
Varsomers137852604
Maprs137852604
PheGenIrs137852604
hapmaprs137852604
1000 genomesrs137852604
hgdprs137852604
ensemblrs137852604
gopubmedrs137852604
geneviewrs137852604
scholarrs137852604
googlers137852604
pharmgkbrs137852604
gwascentralrs137852604
openSNPrs137852604
23andMers137852604
23andMe allrs137852604
SNP Nexus

SNPshotrs137852604
SNPdbers137852604
MSV3drs137852604
GWAS Ctlgrs137852604
Max Magnitude0
OMIM600020
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137852604(T;T)
Alt rs137852604(T;T)
Reference rs137852604(C;C)
Significance Pathogenic
Disease Neurofibrosarcoma
Variation info
Gene MXI1
CLNDBN Neurofibrosarcoma
Reversed 0
HGVS NC_000010.10:g.111988034C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010145.2,