rs16970672

Orientation

plus

Stabilized

plus

Make rs16970672(A;A)

Make rs16970672(A;G)

Make rs16970672(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

77948568

is a	snp
is	mentioned by
dbSNP	rs16970672
dbSNP (classic)	rs16970672
ClinGen	rs16970672
ebi	rs16970672
HLI	rs16970672
Exac	rs16970672
Gnomad	rs16970672
Varsome	rs16970672
LitVar	rs16970672
Map	rs16970672
PheGenI	rs16970672
Biobank	rs16970672
1000 genomes	rs16970672
hgdp	rs16970672
ensembl	rs16970672
geneview	rs16970672
scholar	rs16970672
google	rs16970672
pharmgkb	rs16970672
gwascentral	rs16970672
openSNP	rs16970672
23andMe	rs16970672
SNPshot	rs16970672
SNPdbe	rs16970672
MSV3d	rs16970672
GWAS Ctlg	rs16970672

GMAF

0.3246

Max Magnitude

0

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

GWAS snp
PMID	[PMID 22005930]
Trait
Title	Genome-wide association study of Alzheimer's disease with psychotic symptoms.
Risk Allele
P-val	0.000002
Odds Ratio	1.2900 None