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rs121908661

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908661(C;T)
Make rs121908661(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position68386582
GeneLRP5
is asnp
is mentioned by
dbSNPrs121908661
ebirs121908661
HLIrs121908661
Exacrs121908661
Varsomers121908661
Maprs121908661
PheGenIrs121908661
hapmaprs121908661
1000 genomesrs121908661
hgdprs121908661
ensemblrs121908661
gopubmedrs121908661
geneviewrs121908661
scholarrs121908661
googlers121908661
pharmgkbrs121908661
gwascentralrs121908661
openSNPrs121908661
23andMers121908661
23andMe allrs121908661
SNP Nexus

SNPshotrs121908661
SNPdbers121908661
MSV3drs121908661
GWAS Ctlgrs121908661
Max Magnitude0
OMIM603506
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908661(T;T)
Alt rs121908661(T;T)
Reference rs121908661(C;C)
Significance Pathogenic
Disease Osteoporosis with pseudoglioma
Variation info
Gene LRP5
CLNDBN Osteoporosis with pseudoglioma
Reversed 0
HGVS NC_000011.9:g.68154050C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006647.3,