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rs397514663

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397514663(C;T)
Make rs397514663(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position68403553
GeneLRP5
is asnp
is mentioned by
dbSNPrs397514663
ebirs397514663
HLIrs397514663
Exacrs397514663
Varsomers397514663
Maprs397514663
PheGenIrs397514663
hapmaprs397514663
1000 genomesrs397514663
hgdprs397514663
ensemblrs397514663
gopubmedrs397514663
geneviewrs397514663
scholarrs397514663
googlers397514663
pharmgkbrs397514663
gwascentralrs397514663
openSNPrs397514663
23andMers397514663
23andMe allrs397514663
SNP Nexus

SNPshotrs397514663
SNPdbers397514663
MSV3drs397514663
GWAS Ctlgrs397514663
Max Magnitude0
ClinVar
Risk rs397514663(T;T)
Alt rs397514663(T;T)
Reference rs397514663(C;C)
Significance Pathogenic
Disease Osteoporosis with pseudoglioma
Variation info
Gene LRP5
CLNDBN Osteoporosis with pseudoglioma
Reversed 0
HGVS NC_000011.9:g.68171021C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000033257.4,