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rs3815854

From SNPedia

Orientationminus
Stabilizedminus
Make rs3815854(A;A)
Make rs3815854(A;G)
Make rs3815854(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position219804017
is asnp
is mentioned by
dbSNPrs3815854
dbSNP (classic)rs3815854
ClinGenrs3815854
ebirs3815854
HLIrs3815854
Exacrs3815854
Gnomadrs3815854
Varsomers3815854
LitVarrs3815854
Maprs3815854
PheGenIrs3815854
Biobankrs3815854
1000 genomesrs3815854
hgdprs3815854
ensemblrs3815854
geneviewrs3815854
scholarrs3815854
googlers3815854
pharmgkbrs3815854
gwascentralrs3815854
openSNPrs3815854
23andMers3815854
SNPshotrs3815854
SNPdbers3815854
MSV3drs3815854
GWAS Ctlgrs3815854
GMAF0.4426
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 22863734OA-icon.png]
Trait Orofacial clefts
Title Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.
Risk Allele
P-val 7E-6
Odds Ratio NR NR