rs1861050

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs1861050(C;T)

Make rs1861050(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

15480736

Gene

CC2D2A

is a	snp
is	mentioned by
dbSNP	rs1861050
dbSNP (classic)	rs1861050
ClinGen	rs1861050
ebi	rs1861050
HLI	rs1861050
Exac	rs1861050
Gnomad	rs1861050
Varsome	rs1861050
LitVar	rs1861050
Map	rs1861050
PheGenI	rs1861050
Biobank	rs1861050
1000 genomes	rs1861050
hgdp	rs1861050
ensembl	rs1861050
geneview	rs1861050
scholar	rs1861050
google	rs1861050
pharmgkb	rs1861050
gwascentral	rs1861050
openSNP	rs1861050
23andMe	rs1861050
SNPshot	rs1861050
SNPdbe	rs1861050
MSV3d	rs1861050
GWAS Ctlg	rs1861050

GMAF

0.1107

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 20585324]
Trait	Conduct disorder (case status)
Title	Genome-wide association study of conduct disorder symptomatology
Risk Allele
P-val	0.000008
Odds Ratio	1.63 [1.31-2.01]

ClinVar
Risk	rs1861050(T;T)
Alt	rs1861050(T;T)
Reference	Rs1861050(C;C)
Significance	Other
Disease	not specified Joubert syndrome Meckel-Gruber syndrome
Variation	info
Gene	CC2D2A
CLNDBN	not specified Joubert syndrome Meckel-Gruber syndrome
Reversed	0
HGVS	NC_000004.11:g.15482360C>T
CLNSRC	ClinVar University of Chicago
CLNACC	RCV000114165.3, RCV000269461.1, RCV000329244.1,