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rs121908668

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908668(G;T)
Make rs121908668(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position68357673
GeneLRP5
is asnp
is mentioned by
dbSNPrs121908668
ebirs121908668
HLIrs121908668
Exacrs121908668
Varsomers121908668
Maprs121908668
PheGenIrs121908668
hapmaprs121908668
1000 genomesrs121908668
hgdprs121908668
ensemblrs121908668
gopubmedrs121908668
geneviewrs121908668
scholarrs121908668
googlers121908668
pharmgkbrs121908668
gwascentralrs121908668
openSNPrs121908668
23andMers121908668
23andMe allrs121908668
SNP Nexus

SNPshotrs121908668
SNPdbers121908668
MSV3drs121908668
GWAS Ctlgrs121908668
Max Magnitude0
OMIM603506
Desc
Variant0013
Relatedalso
ClinVar
Risk rs121908668(T;T)
Alt rs121908668(T;T)
Reference rs121908668(G;G)
Significance Pathogenic
Disease High bone mass
Variation info
Gene LRP5
CLNDBN High bone mass
Reversed 0
HGVS NC_000011.9:g.68125141G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006658.3,