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rs9574565

From SNPedia

Orientationplus
Stabilizedplus
Make rs9574565(C;C)
Make rs9574565(C;T)
Make rs9574565(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position80094739
is asnp
is mentioned by
dbSNPrs9574565
ebirs9574565
HLIrs9574565
Exacrs9574565
Varsomers9574565
Maprs9574565
PheGenIrs9574565
hapmaprs9574565
1000 genomesrs9574565
hgdprs9574565
ensemblrs9574565
gopubmedrs9574565
geneviewrs9574565
scholarrs9574565
googlers9574565
pharmgkbrs9574565
gwascentralrs9574565
openSNPrs9574565
23andMers9574565
23andMe allrs9574565
SNP Nexus

SNPshotrs9574565
SNPdbers9574565
MSV3drs9574565
GWAS Ctlgrs9574565
GMAF0.298
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20023658]
Trait Nonsyndromic cleft lip with or without cleft palate
Title Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate
Risk Allele C
P-val 3E-7
Odds Ratio 1.31 [1.01-1.70]

Associated with European Facial Appearance 10.1371/journal.pgen.1002932


GET Evidence
rs9574565
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.611111
summary