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rs866789963

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs866789963(A;A)
Make rs866789963(A;C)
ReferenceGRCh38.p7 38.3/149
Chromosome12
Position12150835
GeneLRP6
is asnp
is mentioned by
dbSNPrs866789963
dbSNP (classic)rs866789963
ClinGenrs866789963
ebirs866789963
HLIrs866789963
Exacrs866789963
Gnomadrs866789963
Varsomers866789963
LitVarrs866789963
Maprs866789963
PheGenIrs866789963
Biobankrs866789963
1000 genomesrs866789963
hgdprs866789963
ensemblrs866789963
geneviewrs866789963
scholarrs866789963
googlers866789963
pharmgkbrs866789963
gwascentralrs866789963
openSNPrs866789963
23andMers866789963
SNPshotrs866789963
SNPdbers866789963
MSV3drs866789963
GWAS Ctlgrs866789963
Max Magnitude0
ClinVar
Risk rs866789963(A;A) rs866789963(T;T)
Alt rs866789963(A;A) rs866789963(T;T)
Reference Rs866789963(C;C)
Significance Probable-Pathogenic
Disease Tooth agenesis
Variation info
Gene LRP6
CLNDBN Tooth agenesis
Reversed 0
HGVS NC_000012.11:g.12303769C>T
CLNSRC
CLNACC RCV000210764.1,