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rs770383372

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs770383372(G;T)
Make rs770383372(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position68357661
GeneLRP5
is asnp
is mentioned by
dbSNPrs770383372
ebirs770383372
HLIrs770383372
Exacrs770383372
Varsomers770383372
Maprs770383372
PheGenIrs770383372
hapmaprs770383372
1000 genomesrs770383372
hgdprs770383372
ensemblrs770383372
gopubmedrs770383372
geneviewrs770383372
scholarrs770383372
googlers770383372
pharmgkbrs770383372
gwascentralrs770383372
openSNPrs770383372
23andMers770383372
23andMe allrs770383372
SNP Nexus

SNPshotrs770383372
SNPdbers770383372
MSV3drs770383372
GWAS Ctlgrs770383372
Max Magnitude0
ClinVar
Risk rs770383372(T;T)
Alt rs770383372(T;T)
Reference rs770383372(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene LRP5
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000011.9:g.68125129G>C
CLNSRC
CLNACC RCV000190810.1,