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rs121908664

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908664(A;A)
Make rs121908664(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position68389949
GeneLRP5
is asnp
is mentioned by
dbSNPrs121908664
ebirs121908664
HLIrs121908664
Exacrs121908664
Varsomers121908664
Maprs121908664
PheGenIrs121908664
hapmaprs121908664
1000 genomesrs121908664
hgdprs121908664
ensemblrs121908664
gopubmedrs121908664
geneviewrs121908664
scholarrs121908664
googlers121908664
pharmgkbrs121908664
gwascentralrs121908664
openSNPrs121908664
23andMers121908664
23andMe allrs121908664
SNP Nexus

SNPshotrs121908664
SNPdbers121908664
MSV3drs121908664
GWAS Ctlgrs121908664
Max Magnitude0
OMIM603506
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121908664(A;A)
Alt rs121908664(A;A)
Reference rs121908664(G;G)
Significance Pathogenic
Disease Osteoporosis with pseudoglioma
Variation info
Gene LRP5
CLNDBN Osteoporosis with pseudoglioma
Reversed 0
HGVS NC_000011.9:g.68157417G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006652.3,