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rs121908667

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908667(A;A)
Make rs121908667(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position68410024
GeneLRP5
is asnp
is mentioned by
dbSNPrs121908667
ebirs121908667
HLIrs121908667
Exacrs121908667
Varsomers121908667
Maprs121908667
PheGenIrs121908667
hapmaprs121908667
1000 genomesrs121908667
hgdprs121908667
ensemblrs121908667
gopubmedrs121908667
geneviewrs121908667
scholarrs121908667
googlers121908667
pharmgkbrs121908667
gwascentralrs121908667
openSNPrs121908667
23andMers121908667
23andMe allrs121908667
SNP Nexus

SNPshotrs121908667
SNPdbers121908667
MSV3drs121908667
GWAS Ctlgrs121908667
Max Magnitude0
OMIM603506
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121908667(A;A)
Alt rs121908667(A;A)
Reference rs121908667(G;G)
Significance Pathogenic
Disease Osteoporosis with pseudoglioma
Variation info
Gene LRP5
CLNDBN Osteoporosis with pseudoglioma
Reversed 0
HGVS NC_000011.9:g.68177492G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006656.3,