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rs121908671

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908671(A;A)
Make rs121908671(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position68357801
GeneLRP5
is asnp
is mentioned by
dbSNPrs121908671
ebirs121908671
HLIrs121908671
Exacrs121908671
Varsomers121908671
Maprs121908671
PheGenIrs121908671
hapmaprs121908671
1000 genomesrs121908671
hgdprs121908671
ensemblrs121908671
gopubmedrs121908671
geneviewrs121908671
scholarrs121908671
googlers121908671
pharmgkbrs121908671
gwascentralrs121908671
openSNPrs121908671
23andMers121908671
23andMe allrs121908671
SNP Nexus

SNPshotrs121908671
SNPdbers121908671
MSV3drs121908671
GWAS Ctlgrs121908671
Max Magnitude0
OMIM603506
Desc
Variant0016
Relatedalso
ClinVar
Risk rs121908671(A;A)
Alt rs121908671(A;A)
Reference rs121908671(G;G)
Significance Pathogenic
Disease Worth disease
Variation info
Gene LRP5
CLNDBN Worth disease
Reversed 0
HGVS NC_000011.9:g.68125269G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006663.2,