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rs387907008

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907008(C;T)
Make rs387907008(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position40688639
GeneMAFB
is asnp
is mentioned by
dbSNPrs387907008
ebirs387907008
HLIrs387907008
Exacrs387907008
Varsomers387907008
Maprs387907008
PheGenIrs387907008
hapmaprs387907008
1000 genomesrs387907008
hgdprs387907008
ensemblrs387907008
gopubmedrs387907008
geneviewrs387907008
scholarrs387907008
googlers387907008
pharmgkbrs387907008
gwascentralrs387907008
openSNPrs387907008
23andMers387907008
23andMe allrs387907008
SNP Nexus

SNPshotrs387907008
SNPdbers387907008
MSV3drs387907008
GWAS Ctlgrs387907008
Max Magnitude0
ClinVar
Risk rs387907008(T;T)
Alt rs387907008(T;T)
Reference rs387907008(C;C)
Significance Pathogenic
Disease Multicentric osteolysis nephropathy
Variation info
Gene MAFB
CLNDBN Multicentric osteolysis nephropathy
Reversed 1
HGVS NC_000020.10:g.39317279G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023751.2,