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rs149645175

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs149645175(C;G)
Make rs149645175(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position68448822
GeneLRP5
is asnp
is mentioned by
dbSNPrs149645175
ebirs149645175
HLIrs149645175
Exacrs149645175
Varsomers149645175
Maprs149645175
PheGenIrs149645175
hapmaprs149645175
1000 genomesrs149645175
hgdprs149645175
ensemblrs149645175
gopubmedrs149645175
geneviewrs149645175
scholarrs149645175
googlers149645175
pharmgkbrs149645175
gwascentralrs149645175
openSNPrs149645175
23andMers149645175
23andMe allrs149645175
SNP Nexus

SNPshotrs149645175
SNPdbers149645175
MSV3drs149645175
GWAS Ctlgrs149645175
Max Magnitude0
ClinVar
Risk rs149645175(G,T;G,T)
Alt rs149645175(G,T;G,T)
Reference rs149645175(C;C)
Significance Pathogenic
Disease Osteoporosis with pseudoglioma
Variation info
Gene LRP5
CLNDBN Osteoporosis with pseudoglioma
Reversed 0
HGVS NC_000011.9:g.68216290C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000033260.4,