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rs4703822

From SNPedia

Orientationplus
Stabilizedplus
Make rs4703822(A;A)
Make rs4703822(A;G)
Make rs4703822(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position81115402
GeneRASGRF2
is asnp
is mentioned by
dbSNPrs4703822
ebirs4703822
HLIrs4703822
Exacrs4703822
Varsomers4703822
Maprs4703822
PheGenIrs4703822
hapmaprs4703822
1000 genomesrs4703822
hgdprs4703822
ensemblrs4703822
gopubmedrs4703822
geneviewrs4703822
scholarrs4703822
googlers4703822
pharmgkbrs4703822
gwascentralrs4703822
openSNPrs4703822
23andMers4703822
23andMe allrs4703822
SNP Nexus

SNPshotrs4703822
SNPdbers4703822
MSV3drs4703822
GWAS Ctlgrs4703822
GMAF0.2635
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 0.000004
Odds Ratio 1.5900 None