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rs1489032

From SNPedia

Orientationplus
Make rs1489032(C;C)
Make rs1489032(C;T)
Make rs1489032(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position111333764
GeneLOC105374039
is asnp
is mentioned by
dbSNPrs1489032
ebirs1489032
HLIrs1489032
Exacrs1489032
Varsomers1489032
Maprs1489032
PheGenIrs1489032
hapmaprs1489032
1000 genomesrs1489032
hgdprs1489032
ensemblrs1489032
gopubmedrs1489032
geneviewrs1489032
scholarrs1489032
googlers1489032
pharmgkbrs1489032
gwascentralrs1489032
openSNPrs1489032
23andMers1489032
23andMe allrs1489032
SNP Nexus

SNPshotrs1489032
SNPdbers1489032
MSV3drs1489032
GWAS Ctlgrs1489032
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 27318898] [Association study between candidate genes involved in cell-cell adhesion and non-syndromic cleft lip with or without cleft palate in Chinese population].