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rs397514664

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397514664(C;T)
Make rs397514664(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position68386445
GeneLRP5
is asnp
is mentioned by
dbSNPrs397514664
ebirs397514664
HLIrs397514664
Exacrs397514664
Varsomers397514664
Maprs397514664
PheGenIrs397514664
hapmaprs397514664
1000 genomesrs397514664
hgdprs397514664
ensemblrs397514664
gopubmedrs397514664
geneviewrs397514664
scholarrs397514664
googlers397514664
pharmgkbrs397514664
gwascentralrs397514664
openSNPrs397514664
23andMers397514664
23andMe allrs397514664
SNP Nexus

SNPshotrs397514664
SNPdbers397514664
MSV3drs397514664
GWAS Ctlgrs397514664
Max Magnitude0
ClinVar
Risk rs397514664(T;T)
Alt rs397514664(T;T)
Reference rs397514664(C;C)
Significance Pathogenic
Disease Osteoporosis with pseudoglioma
Variation info
Gene LRP5
CLNDBN Osteoporosis with pseudoglioma
Reversed 0
HGVS NC_000011.9:g.68153913C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000033258.3,