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rs4132699

From SNPedia

Orientationplus
Stabilizedplus
Make rs4132699(A;A)
Make rs4132699(A;C)
Make rs4132699(C;C)
ReferenceGRCh38 38.1/141
Chromosome9
Position89421512
GeneSEMA4D
is asnp
is mentioned by
dbSNPrs4132699
dbSNP (classic)rs4132699
ClinGenrs4132699
ebirs4132699
HLIrs4132699
Exacrs4132699
Gnomadrs4132699
Varsomers4132699
LitVarrs4132699
Maprs4132699
PheGenIrs4132699
Biobankrs4132699
1000 genomesrs4132699
hgdprs4132699
ensemblrs4132699
geneviewrs4132699
scholarrs4132699
googlers4132699
pharmgkbrs4132699
gwascentralrs4132699
openSNPrs4132699
23andMers4132699
SNPshotrs4132699
SNPdbers4132699
MSV3drs4132699
GWAS Ctlgrs4132699
GMAF0.382
Max Magnitude0
? (A;A) (A;C) (C;C) 28


GWAS snp
PMID [PMID 22863734OA-icon.png]
Trait Orofacial clefts
Title Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.
Risk Allele
P-val 5E-7
Odds Ratio NR NR