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rs387907007

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907007(C;T)
Make rs387907007(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position40688640
GeneMAFB
is asnp
is mentioned by
dbSNPrs387907007
ebirs387907007
HLIrs387907007
Exacrs387907007
Varsomers387907007
Maprs387907007
PheGenIrs387907007
hapmaprs387907007
1000 genomesrs387907007
hgdprs387907007
ensemblrs387907007
gopubmedrs387907007
geneviewrs387907007
scholarrs387907007
googlers387907007
pharmgkbrs387907007
gwascentralrs387907007
openSNPrs387907007
23andMers387907007
23andMe allrs387907007
SNP Nexus

SNPshotrs387907007
SNPdbers387907007
MSV3drs387907007
GWAS Ctlgrs387907007
Max Magnitude0
ClinVar
Risk rs387907007(T;T)
Alt rs387907007(T;T)
Reference rs387907007(C;C)
Significance Pathogenic
Disease Multicentric osteolysis nephropathy
Variation info
Gene MAFB
CLNDBN Multicentric osteolysis nephropathy
Reversed 1
HGVS NC_000020.10:g.39317280G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023750.2,