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rs766589610

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs766589610(C;T)
Make rs766589610(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position68357846
GeneLRP5
is asnp
is mentioned by
dbSNPrs766589610
ebirs766589610
HLIrs766589610
Exacrs766589610
Varsomers766589610
Maprs766589610
PheGenIrs766589610
hapmaprs766589610
1000 genomesrs766589610
hgdprs766589610
ensemblrs766589610
gopubmedrs766589610
geneviewrs766589610
scholarrs766589610
googlers766589610
pharmgkbrs766589610
gwascentralrs766589610
openSNPrs766589610
23andMers766589610
23andMe allrs766589610
SNP Nexus

SNPshotrs766589610
SNPdbers766589610
MSV3drs766589610
GWAS Ctlgrs766589610
Max Magnitude0
ClinVar
Risk rs766589610(T;T)
Alt rs766589610(T;T)
Reference rs766589610(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LRP5
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.68125314C>T
CLNSRC
CLNACC RCV000171198.1,