Have questions? Visit https://www.reddit.com/r/SNPedia

rs121908663

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908663(C;T)
Make rs121908663(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position68413742
GeneLRP5
is asnp
is mentioned by
dbSNPrs121908663
ebirs121908663
HLIrs121908663
Exacrs121908663
Varsomers121908663
Maprs121908663
PheGenIrs121908663
hapmaprs121908663
1000 genomesrs121908663
hgdprs121908663
ensemblrs121908663
gopubmedrs121908663
geneviewrs121908663
scholarrs121908663
googlers121908663
pharmgkbrs121908663
gwascentralrs121908663
openSNPrs121908663
23andMers121908663
23andMe allrs121908663
SNP Nexus

SNPshotrs121908663
SNPdbers121908663
MSV3drs121908663
GWAS Ctlgrs121908663
Max Magnitude0
OMIM603506
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121908663(T;T)
Alt rs121908663(T;T)
Reference rs121908663(C;C)
Significance Pathogenic
Disease Osteoporosis with pseudoglioma
Variation info
Gene LRP5
CLNDBN Osteoporosis with pseudoglioma
Reversed 0
HGVS NC_000011.9:g.68181210C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006650.3,