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rs869320635

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869320635(-;-)
Make rs869320635(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position12121375
GeneLRP6
is asnp
is mentioned by
dbSNPrs869320635
dbSNP (classic)rs869320635
ClinGenrs869320635
ebirs869320635
HLIrs869320635
Exacrs869320635
Gnomadrs869320635
Varsomers869320635
LitVarrs869320635
Maprs869320635
PheGenIrs869320635
Biobankrs869320635
1000 genomesrs869320635
hgdprs869320635
ensemblrs869320635
geneviewrs869320635
scholarrs869320635
googlers869320635
pharmgkbrs869320635
gwascentralrs869320635
openSNPrs869320635
23andMers869320635
SNPshotrs869320635
SNPdbers869320635
MSV3drs869320635
GWAS Ctlgrs869320635
Max Magnitude0
ClinVar
Risk rs869320635(-;-)
Alt rs869320635(-;-)
Reference Rs869320635(C;C)
Significance Pathogenic
Disease Orofacial clefting Tooth agenesis
Variation info
Gene LRP6
CLNDBN Orofacial clefting Tooth agenesis
Reversed 1
HGVS NC_000012.11:g.12274309delG
CLNSRC
CLNACC RCV000210778.1,