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rs121908666

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908666(G;T)
Make rs121908666(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position68389921
GeneLRP5
is asnp
is mentioned by
dbSNPrs121908666
ebirs121908666
HLIrs121908666
Exacrs121908666
Varsomers121908666
Maprs121908666
PheGenIrs121908666
hapmaprs121908666
1000 genomesrs121908666
hgdprs121908666
ensemblrs121908666
gopubmedrs121908666
geneviewrs121908666
scholarrs121908666
googlers121908666
pharmgkbrs121908666
gwascentralrs121908666
openSNPrs121908666
23andMers121908666
23andMe allrs121908666
SNP Nexus

SNPshotrs121908666
SNPdbers121908666
MSV3drs121908666
GWAS Ctlgrs121908666
Max Magnitude0
OMIM603506
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121908666(T;T)
Alt rs121908666(T;T)
Reference rs121908666(G;G)
Significance Pathogenic
Disease Osteoporosis with pseudoglioma
Variation info
Gene LRP5
CLNDBN Osteoporosis with pseudoglioma
Reversed 0
HGVS NC_000011.9:g.68157389G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006655.3,