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rs137852864

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852864(A;A)
Make rs137852864(A;C)
ReferenceGRCh38 38.1/141
Chromosome14
Position45173065
GeneFANCM
is asnp
is mentioned by
dbSNPrs137852864
ebirs137852864
HLIrs137852864
Exacrs137852864
Varsomers137852864
Maprs137852864
PheGenIrs137852864
hapmaprs137852864
1000 genomesrs137852864
hgdprs137852864
ensemblrs137852864
gopubmedrs137852864
geneviewrs137852864
scholarrs137852864
googlers137852864
pharmgkbrs137852864
gwascentralrs137852864
openSNPrs137852864
23andMers137852864
23andMe allrs137852864
SNP Nexus

SNPshotrs137852864
SNPdbers137852864
MSV3drs137852864
GWAS Ctlgrs137852864
Max Magnitude0
OMIM609644
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137852864(A;A)
Alt rs137852864(A;A)
Reference rs137852864(C;C)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCM
CLNDBN Fanconi anemia, complementation group M
Reversed 0
HGVS NC_000014.8:g.45642268C>A
CLNSRC Fanconi Anaemia Mutation Database (FANCM) OMIM Allelic Variant
CLNACC RCV000001665.4,