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rs10905099

From SNPedia

Orientationplus
Stabilizedplus
Make rs10905099(A;A)
Make rs10905099(A;G)
Make rs10905099(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position7047054
is asnp
is mentioned by
dbSNPrs10905099
ebirs10905099
HLIrs10905099
Exacrs10905099
Varsomers10905099
Maprs10905099
PheGenIrs10905099
hapmaprs10905099
1000 genomesrs10905099
hgdprs10905099
ensemblrs10905099
gopubmedrs10905099
geneviewrs10905099
scholarrs10905099
googlers10905099
pharmgkbrs10905099
gwascentralrs10905099
openSNPrs10905099
23andMers10905099
23andMe allrs10905099
SNP Nexus

SNPshotrs10905099
SNPdbers10905099
MSV3drs10905099
GWAS Ctlgrs10905099
GMAF0.06152
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 0.000008
Odds Ratio 3.4500 None