rs1861046

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	1

Make rs1861046(A;A)

Make rs1861046(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

15396282

Gene	C1QTNF7, LOC101929095

is a	snp
is	mentioned by
dbSNP	rs1861046
dbSNP (classic)	rs1861046
ClinGen	rs1861046
ebi	rs1861046
HLI	rs1861046
Exac	rs1861046
Gnomad	rs1861046
Varsome	rs1861046
LitVar	rs1861046
Map	rs1861046
PheGenI	rs1861046
Biobank	rs1861046
1000 genomes	rs1861046
hgdp	rs1861046
ensembl	rs1861046
geneview	rs1861046
scholar	rs1861046
google	rs1861046
pharmgkb	rs1861046
gwascentral	rs1861046
openSNP	rs1861046
23andMe	rs1861046
SNPshot	rs1861046
SNPdbe	rs1861046
MSV3d	rs1861046
GWAS Ctlg	rs1861046

GMAF

0.1478

Max Magnitude

1

?	(A;A) (A;G) (G;G)	28

GWAS snp
PMID	[PMID 20585324]
Trait	Conduct disorder (case status)
Title	Genome-wide association study of conduct disorder symptomatology
Risk Allele
P-val	6E-8
Odds Ratio	1.65 [1.38-1.98]