Have questions? Visit https://www.reddit.com/r/SNPedia

rs1450100

From SNPedia

Orientationminus
Stabilizedminus
Make rs1450100(A;A)
Make rs1450100(A;C)
Make rs1450100(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position7496515
GeneGRM7
is asnp
is mentioned by
dbSNPrs1450100
ebirs1450100
HLIrs1450100
Exacrs1450100
Varsomers1450100
Maprs1450100
PheGenIrs1450100
hapmaprs1450100
1000 genomesrs1450100
hgdprs1450100
ensemblrs1450100
gopubmedrs1450100
geneviewrs1450100
scholarrs1450100
googlers1450100
pharmgkbrs1450100
gwascentralrs1450100
openSNPrs1450100
23andMers1450100
23andMe allrs1450100
SNP Nexus

SNPshotrs1450100
SNPdbers1450100
MSV3drs1450100
GWAS Ctlgrs1450100
GMAF0.3393
Max Magnitude
? (A;A) (A;C) (C;C) 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 1.5400 None