Have questions? Visit https://www.reddit.com/r/SNPedia

rs121908672

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908672(C;T)
Make rs121908672(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position68357802
GeneLRP5
is asnp
is mentioned by
dbSNPrs121908672
ebirs121908672
HLIrs121908672
Exacrs121908672
Varsomers121908672
Maprs121908672
PheGenIrs121908672
hapmaprs121908672
1000 genomesrs121908672
hgdprs121908672
ensemblrs121908672
gopubmedrs121908672
geneviewrs121908672
scholarrs121908672
googlers121908672
pharmgkbrs121908672
gwascentralrs121908672
openSNPrs121908672
23andMers121908672
23andMe allrs121908672
SNP Nexus

SNPshotrs121908672
SNPdbers121908672
MSV3drs121908672
GWAS Ctlgrs121908672
Max Magnitude0
OMIM603506
Desc
Variant0017
Relatedalso
ClinVar
Risk rs121908672(T;T)
Alt rs121908672(T;T)
Reference rs121908672(C;C)
Significance Pathogenic
Disease Worth disease
Variation info
Gene LRP5
CLNDBN Worth disease
Reversed 0
HGVS NC_000011.9:g.68125270C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006664.2,