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rs121908660

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908660(A;A)
Make rs121908660(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position68312743
GeneLRP5
is asnp
is mentioned by
dbSNPrs121908660
ebirs121908660
HLIrs121908660
Exacrs121908660
Varsomers121908660
Maprs121908660
PheGenIrs121908660
hapmaprs121908660
1000 genomesrs121908660
hgdprs121908660
ensemblrs121908660
gopubmedrs121908660
geneviewrs121908660
scholarrs121908660
googlers121908660
pharmgkbrs121908660
gwascentralrs121908660
openSNPrs121908660
23andMers121908660
23andMe allrs121908660
SNP Nexus

SNPshotrs121908660
SNPdbers121908660
MSV3drs121908660
GWAS Ctlgrs121908660
Max Magnitude0
OMIM603506
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908660(A;A)
Alt rs121908660(A;A)
Reference rs121908660(G;G)
Significance Pathogenic
Disease Osteoporosis with pseudoglioma
Variation info
Gene LRP5
CLNDBN Osteoporosis with pseudoglioma
Reversed 0
HGVS NC_000011.9:g.68080211G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006646.3,