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rs3764628

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs3764628(A;A)
Make rs3764628(A;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position18636795
GeneKLHL26
is asnp
is mentioned by
dbSNPrs3764628
ebirs3764628
HLIrs3764628
Exacrs3764628
Varsomers3764628
Maprs3764628
PheGenIrs3764628
hapmaprs3764628
1000 genomesrs3764628
hgdprs3764628
ensemblrs3764628
gopubmedrs3764628
geneviewrs3764628
scholarrs3764628
googlers3764628
pharmgkbrs3764628
gwascentralrs3764628
openSNPrs3764628
23andMers3764628
23andMe allrs3764628
SNP Nexus

SNPshotrs3764628
SNPdbers3764628
MSV3drs3764628
GWAS Ctlgrs3764628
GMAF0.09275
Max Magnitude0
? (A;A) (A;C) (C;C) 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 0.000004
Odds Ratio 1.8900 None