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rs17138064

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs17138064(A;A)
Make rs17138064(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position36831827
is asnp
is mentioned by
dbSNPrs17138064
ebirs17138064
HLIrs17138064
Exacrs17138064
Varsomers17138064
Maprs17138064
PheGenIrs17138064
hapmaprs17138064
1000 genomesrs17138064
hgdprs17138064
ensemblrs17138064
gopubmedrs17138064
geneviewrs17138064
scholarrs17138064
googlers17138064
pharmgkbrs17138064
gwascentralrs17138064
openSNPrs17138064
23andMers17138064
23andMe allrs17138064
SNP Nexus

SNPshotrs17138064
SNPdbers17138064
MSV3drs17138064
GWAS Ctlgrs17138064
GMAF0.08678
Max Magnitude0
? (A;A) (A;G) (G;G) 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 5E-7
Odds Ratio 1.9200 None