rs16891867

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common genotype

Make rs16891867(A;G)

Make rs16891867(G;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

15395740

Gene	C1QTNF7, LOC101929095

is a	snp
is	mentioned by
dbSNP	rs16891867
dbSNP (classic)	rs16891867
ClinGen	rs16891867
ebi	rs16891867
HLI	rs16891867
Exac	rs16891867
Gnomad	rs16891867
Varsome	rs16891867
LitVar	rs16891867
Map	rs16891867
PheGenI	rs16891867
Biobank	rs16891867
1000 genomes	rs16891867
hgdp	rs16891867
ensembl	rs16891867
geneview	rs16891867
scholar	rs16891867
google	rs16891867
pharmgkb	rs16891867
gwascentral	rs16891867
openSNP	rs16891867
23andMe	rs16891867
SNPshot	rs16891867
SNPdbe	rs16891867
MSV3d	rs16891867
GWAS Ctlg	rs16891867

GMAF

0.1478

Max Magnitude

0

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

GWAS snp
PMID	[PMID 20585324]
Trait	Conduct disorder (symptom count)
Title	Genome-wide association study of conduct disorder symptomatology
Risk Allele
P-val	3E-9
Odds Ratio	0.15 [NR] unit increase