rs16961557

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs16961557(A;G)

Make rs16961557(G;G)

Reference

GRCh38 38.1/141

Chromosome

15

Position

48755931

Gene

CEP152

is a	snp
is	mentioned by
dbSNP	rs16961557
dbSNP (classic)	rs16961557
ClinGen	rs16961557
ebi	rs16961557
HLI	rs16961557
Exac	rs16961557
Gnomad	rs16961557
Varsome	rs16961557
LitVar	rs16961557
Map	rs16961557
PheGenI	rs16961557
Biobank	rs16961557
1000 genomes	rs16961557
hgdp	rs16961557
ensembl	rs16961557
geneview	rs16961557
scholar	rs16961557
google	rs16961557
pharmgkb	rs16961557
gwascentral	rs16961557
openSNP	rs16961557
23andMe	rs16961557
SNPshot	rs16961557
SNPdbe	rs16961557
MSV3d	rs16961557
GWAS Ctlg	rs16961557

GMAF

0.03168

Max Magnitude

0

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

GWAS snp
PMID	[PMID 23251661]
Trait	Obesity-related traits
Title	Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
Risk Allele	G
P-val	5E-6
Odds Ratio	.03 [NR] cm increase

ClinVar
Risk	rs16961557(G;G)
Alt	rs16961557(G;G)
Reference	Rs16961557(A;A)
Significance	Probable-non-pathogenic
Disease	not specified Primary Microcephaly Seckel syndrome
Variation	info
Gene	CEP152
CLNDBN	not specified Primary Microcephaly, Recessive Seckel syndrome
Reversed	0
HGVS	NC_000015.9:g.49048128A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000145626.1, RCV000273027.1, RCV000330394.1,