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rs387906883

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906883(C;C)
Make rs387906883(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position46875946
GeneLRP4
is asnp
is mentioned by
dbSNPrs387906883
ClinGenrs387906883
ebirs387906883
HLIrs387906883
Exacrs387906883
Varsomers387906883
Maprs387906883
PheGenIrs387906883
hapmaprs387906883
1000 genomesrs387906883
hgdprs387906883
ensemblrs387906883
gopubmedrs387906883
geneviewrs387906883
scholarrs387906883
googlers387906883
pharmgkbrs387906883
gwascentralrs387906883
openSNPrs387906883
23andMers387906883
23andMe allrs387906883
SNP Nexus

SNPshotrs387906883
SNPdbers387906883
MSV3drs387906883
GWAS Ctlgrs387906883
Max Magnitude0
ClinVar
Risk rs387906883(C;C) rs387906883(T;T)
Alt rs387906883(C;C) rs387906883(T;T)
Reference Rs387906883(G;G)
Significance Pathogenic
Disease Sclerosteosis 2 not provided
Variation info
Gene LRP4
CLNDBN Sclerosteosis 2 not provided
Reversed 1
HGVS NC_000011.9:g.46897497C>G
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000023363.3, RCV000490108.1,