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rs7632427

From SNPedia

Orientationplus
Stabilizedplus
Make rs7632427(C;C)
Make rs7632427(C;T)
Make rs7632427(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position89485227
is asnp
is mentioned by
dbSNPrs7632427
ebirs7632427
HLIrs7632427
Exacrs7632427
Varsomers7632427
Maprs7632427
PheGenIrs7632427
hapmaprs7632427
1000 genomesrs7632427
hgdprs7632427
ensemblrs7632427
gopubmedrs7632427
geneviewrs7632427
scholarrs7632427
googlers7632427
pharmgkbrs7632427
gwascentralrs7632427
openSNPrs7632427
23andMers7632427
23andMe allrs7632427
SNP Nexus

SNPshotrs7632427
SNPdbers7632427
MSV3drs7632427
GWAS Ctlgrs7632427
GMAF0.3884
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 23536526] Association and cumulative effects of GWAS-identified genetic variants for nonsyndromic orofacial clefts in a Chinese population

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 T
P-val 4E-8
Odds Ratio 1.37 [1.20-1.55]


[PMID 25786657OA-icon.png] Replication of 13q31.1 association in nonsyndromic cleft lip with cleft palate in Europeans