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rs10863790

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs10863790(A;C)
Make rs10863790(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position209814702
is asnp
is mentioned by
dbSNPrs10863790
ebirs10863790
HLIrs10863790
Exacrs10863790
Varsomers10863790
Maprs10863790
PheGenIrs10863790
hapmaprs10863790
1000 genomesrs10863790
hgdprs10863790
ensemblrs10863790
gopubmedrs10863790
geneviewrs10863790
scholarrs10863790
googlers10863790
pharmgkbrs10863790
gwascentralrs10863790
openSNPrs10863790
23andMers10863790
23andMe allrs10863790
SNP Nexus

SNPshotrs10863790
SNPdbers10863790
MSV3drs10863790
GWAS Ctlgrs10863790
GMAF0.1373
Max Magnitude0
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 20436469OA-icon.png]
Trait Cleft lip
Title A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4
Risk Allele
P-val 1E-14
Odds Ratio 1.72 [1.49-1.98]