Have questions? Visit https://www.reddit.com/r/SNPedia

rs17079928

From SNPedia

Orientationplus
Stabilizedplus
Make rs17079928(A;A)
Make rs17079928(A;G)
Make rs17079928(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position24080089
GeneSPATA13
is asnp
is mentioned by
dbSNPrs17079928
ebirs17079928
HLIrs17079928
Exacrs17079928
Varsomers17079928
Maprs17079928
PheGenIrs17079928
hapmaprs17079928
1000 genomesrs17079928
hgdprs17079928
ensemblrs17079928
gopubmedrs17079928
geneviewrs17079928
scholarrs17079928
googlers17079928
pharmgkbrs17079928
gwascentralrs17079928
openSNPrs17079928
23andMers17079928
23andMe allrs17079928
SNP Nexus

SNPshotrs17079928
SNPdbers17079928
MSV3drs17079928
GWAS Ctlgrs17079928
GMAF0.2576
Max Magnitude
? (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 0.000006
Odds Ratio 1.3300 None