rs1183910

Orientation

minus

Stabilized

minus

Make rs1183910(C;C)

Make rs1183910(C;T)

Make rs1183910(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

120983004

Gene

HNF1A

is a	snp
is	mentioned by
dbSNP	rs1183910
dbSNP (classic)	rs1183910
ClinGen	rs1183910
ebi	rs1183910
HLI	rs1183910
Exac	rs1183910
Gnomad	rs1183910
Varsome	rs1183910
LitVar	rs1183910
Map	rs1183910
PheGenI	rs1183910
Biobank	rs1183910
1000 genomes	rs1183910
hgdp	rs1183910
ensembl	rs1183910
geneview	rs1183910
scholar	rs1183910
google	rs1183910
pharmgkb	rs1183910
gwascentral	rs1183910
openSNP	rs1183910
23andMe	rs1183910
SNPshot	rs1183910
SNPdbe	rs1183910
MSV3d	rs1183910
GWAS Ctlg	rs1183910

GMAF

0.3039

Max Magnitude

0

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

23andMe blog each rs1183910(T) lowered CRP by 13.8% also associated with higher total cholesterol, LDL choesterol and HDL cholesterol.

[PMID 19567438] Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease

GWAS snp
PMID	[PMID 21300955]
Trait
Title	Meta-Analysis of Genome-Wide Association Studies in >80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels
Risk Allele	G
P-val	2E-124
Odds Ratio	0.1490 [0.14-0.16] unit increase

[PMID 18439552] Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein.

GWAS snp
PMID	[PMID 23844046]
Trait	C-reactive protein
Title	Are C-reactive protein associated genetic variants associated with serum levels and retinal markers of microvascular pathology in Asian populations from Singapore?
Risk Allele	G
P-val	4E-12
Odds Ratio	.05 [NR] unit increase