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rs387906884

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906884(C;T)
Make rs387906884(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position46876494
GeneLRP4
is asnp
is mentioned by
dbSNPrs387906884
ebirs387906884
HLIrs387906884
Exacrs387906884
Varsomers387906884
Maprs387906884
PheGenIrs387906884
hapmaprs387906884
1000 genomesrs387906884
hgdprs387906884
ensemblrs387906884
gopubmedrs387906884
geneviewrs387906884
scholarrs387906884
googlers387906884
pharmgkbrs387906884
gwascentralrs387906884
openSNPrs387906884
23andMers387906884
23andMe allrs387906884
SNP Nexus

SNPshotrs387906884
SNPdbers387906884
MSV3drs387906884
GWAS Ctlgrs387906884
Max Magnitude0
ClinVar
Risk rs387906884(T;T)
Alt rs387906884(T;T)
Reference rs387906884(C;C)
Significance Pathogenic
Disease Sclerosteosis 2
Variation info
Gene LRP4
CLNDBN Sclerosteosis 2
Reversed 1
HGVS NC_000011.9:g.46898045G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023364.3,