rs35444

Orientation

minus

Stabilized

minus

Make rs35444(C;C)

Make rs35444(C;T)

Make rs35444(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

115114632

is a	snp
is	mentioned by
dbSNP	rs35444
dbSNP (classic)	rs35444
ClinGen	rs35444
ebi	rs35444
HLI	rs35444
Exac	rs35444
Gnomad	rs35444
Varsome	rs35444
LitVar	rs35444
Map	rs35444
PheGenI	rs35444
Biobank	rs35444
1000 genomes	rs35444
hgdp	rs35444
ensembl	rs35444
geneview	rs35444
scholar	rs35444
google	rs35444
pharmgkb	rs35444
gwascentral	rs35444
openSNP	rs35444
23andMe	rs35444
SNPshot	rs35444
SNPdbe	rs35444
MSV3d	rs35444
GWAS Ctlg	rs35444

GMAF

0.3691

Max Magnitude

0

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

GWAS snp
PMID	[PMID 21572416]
Trait
Title	Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians.
Risk Allele	A
P-val	8E-7
Odds Ratio	0.6300 [0.38-0.88] mm Hg increase