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rs17085106

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs17085106(G;T)
Make rs17085106(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position71771837
is asnp
is mentioned by
dbSNPrs17085106
ebirs17085106
HLIrs17085106
Exacrs17085106
Varsomers17085106
Maprs17085106
PheGenIrs17085106
hapmaprs17085106
1000 genomesrs17085106
hgdprs17085106
ensemblrs17085106
gopubmedrs17085106
geneviewrs17085106
scholarrs17085106
googlers17085106
pharmgkbrs17085106
gwascentralrs17085106
openSNPrs17085106
23andMers17085106
23andMe allrs17085106
SNP Nexus

SNPshotrs17085106
SNPdbers17085106
MSV3drs17085106
GWAS Ctlgrs17085106
GMAF0.06015
Max Magnitude0
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 19656524]
Trait Nonsyndromic cleft lip with or without cleft palate
Title A Genome-Wide Association Study Identifies a Locus for Nonsyndromic Cleft Lip with or without Cleft Palate on 8q24
Risk Allele
P-val 4E-8
Odds Ratio 4.07 [2.37-7.00]


GET Evidence
rs17085106
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0546875
summary



[PMID 26198054] Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Brazilian population with high African ancestry