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rs387907004

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387907004(A;C)
Make rs387907004(C;C)
ReferenceGRCh38 38.1/141
Chromosome20
Position40688667
GeneMAFB
is asnp
is mentioned by
dbSNPrs387907004
ebirs387907004
HLIrs387907004
Exacrs387907004
Varsomers387907004
Maprs387907004
PheGenIrs387907004
hapmaprs387907004
1000 genomesrs387907004
hgdprs387907004
ensemblrs387907004
gopubmedrs387907004
geneviewrs387907004
scholarrs387907004
googlers387907004
pharmgkbrs387907004
gwascentralrs387907004
openSNPrs387907004
23andMers387907004
23andMe allrs387907004
SNP Nexus

SNPshotrs387907004
SNPdbers387907004
MSV3drs387907004
GWAS Ctlgrs387907004
Max Magnitude0
ClinVar
Risk rs387907004(C;C)
Alt rs387907004(C;C)
Reference rs387907004(A;A)
Significance Pathogenic
Disease Multicentric osteolysis nephropathy
Variation info
Gene MAFB
CLNDBN Multicentric osteolysis nephropathy
Reversed 1
HGVS NC_000020.10:g.39317307T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023747.3,