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rs121908665

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908665(C;T)
Make rs121908665(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position68403606
GeneLRP5
is asnp
is mentioned by
dbSNPrs121908665
ebirs121908665
HLIrs121908665
Exacrs121908665
Varsomers121908665
Maprs121908665
PheGenIrs121908665
hapmaprs121908665
1000 genomesrs121908665
hgdprs121908665
ensemblrs121908665
gopubmedrs121908665
geneviewrs121908665
scholarrs121908665
googlers121908665
pharmgkbrs121908665
gwascentralrs121908665
openSNPrs121908665
23andMers121908665
23andMe allrs121908665
SNP Nexus

SNPshotrs121908665
SNPdbers121908665
MSV3drs121908665
GWAS Ctlgrs121908665
Max Magnitude0
OMIM603506
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121908665(T;T)
Alt rs121908665(T;T)
Reference rs121908665(C;C)
Significance Pathogenic
Disease Osteoporosis with pseudoglioma
Variation info
Gene LRP5
CLNDBN Osteoporosis with pseudoglioma
Reversed 0
HGVS NC_000011.9:g.68171074C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006653.3,