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rs17760296

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common on affy axiom data
Make rs17760296(G;G)
Make rs17760296(G;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position56538256
is asnp
is mentioned by
dbSNPrs17760296
ebirs17760296
HLIrs17760296
Exacrs17760296
Varsomers17760296
Maprs17760296
PheGenIrs17760296
hapmaprs17760296
1000 genomesrs17760296
hgdprs17760296
ensemblrs17760296
gopubmedrs17760296
geneviewrs17760296
scholarrs17760296
googlers17760296
pharmgkbrs17760296
gwascentralrs17760296
openSNPrs17760296
23andMers17760296
23andMe allrs17760296
SNP Nexus

SNPshotrs17760296
SNPdbers17760296
MSV3drs17760296
GWAS Ctlgrs17760296
GMAF0.08632
Max Magnitude0
? (G;G) (G;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 G
P-val 0.000007
Odds Ratio 1.50 [1.32-1.69]


GET Evidence
rs17760296
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.132812
summary