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rs1329189

From SNPedia

Orientationplus
Stabilizedplus
Make rs1329189(C;C)
Make rs1329189(C;T)
Make rs1329189(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position128200108
is asnp
is mentioned by
dbSNPrs1329189
ebirs1329189
HLIrs1329189
Exacrs1329189
Varsomers1329189
Maprs1329189
PheGenIrs1329189
hapmaprs1329189
1000 genomesrs1329189
hgdprs1329189
ensemblrs1329189
gopubmedrs1329189
geneviewrs1329189
scholarrs1329189
googlers1329189
pharmgkbrs1329189
gwascentralrs1329189
openSNPrs1329189
23andMers1329189
23andMe allrs1329189
SNP Nexus

SNPshotrs1329189
SNPdbers1329189
MSV3drs1329189
GWAS Ctlgrs1329189
GMAF0.3131
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22419666OA-icon.png]
Trait
Title Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts.
Risk Allele
P-val 0.000005
Odds Ratio 1.3000 None