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rs387907006

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907006(C;T)
Make rs387907006(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position40688642
GeneMAFB
is asnp
is mentioned by
dbSNPrs387907006
ebirs387907006
HLIrs387907006
Exacrs387907006
Varsomers387907006
Maprs387907006
PheGenIrs387907006
hapmaprs387907006
1000 genomesrs387907006
hgdprs387907006
ensemblrs387907006
gopubmedrs387907006
geneviewrs387907006
scholarrs387907006
googlers387907006
pharmgkbrs387907006
gwascentralrs387907006
openSNPrs387907006
23andMers387907006
23andMe allrs387907006
SNP Nexus

SNPshotrs387907006
SNPdbers387907006
MSV3drs387907006
GWAS Ctlgrs387907006
Max Magnitude0
ClinVar
Risk rs387907006(T;T)
Alt rs387907006(T;T)
Reference rs387907006(C;C)
Significance Pathogenic
Disease Multicentric osteolysis nephropathy
Variation info
Gene MAFB
CLNDBN Multicentric osteolysis nephropathy
Reversed 1
HGVS NC_000020.10:g.39317282G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023749.2,