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

rs121908662

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(CTG;CTG) 0 common in clinvar
Make rs121908662(-;-)
Make rs121908662(-;T)
Make rs121908662(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position68409973
GeneLRP5
is asnp
is mentioned by
dbSNPrs121908662
ebirs121908662
HLIrs121908662
Exacrs121908662
Varsomers121908662
Maprs121908662
PheGenIrs121908662
hapmaprs121908662
1000 genomesrs121908662
hgdprs121908662
ensemblrs121908662
gopubmedrs121908662
geneviewrs121908662
scholarrs121908662
googlers121908662
pharmgkbrs121908662
gwascentralrs121908662
openSNPrs121908662
23andMers121908662
23andMe allrs121908662
SNP Nexus

SNPshotrs121908662
SNPdbers121908662
MSV3drs121908662
GWAS Ctlgrs121908662
Max Magnitude0
OMIM603506
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121908662(T;T)
Alt rs121908662(T;T)
Reference rs121908662(CTG;CTG)
Significance Pathogenic
Disease Osteoporosis with pseudoglioma
Variation info
Gene LRP5
CLNDBN Osteoporosis with pseudoglioma
Reversed 0
HGVS NC_000011.9:g.68177441dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000006649.3,