rs7953249

Orientation

plus

Stabilized

plus

Make rs7953249(A;A)

Make rs7953249(A;G)

Make rs7953249(G;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

120965921

is a	snp
is	mentioned by
dbSNP	rs7953249
dbSNP (classic)	rs7953249
ClinGen	rs7953249
ebi	rs7953249
HLI	rs7953249
Exac	rs7953249
Gnomad	rs7953249
Varsome	rs7953249
LitVar	rs7953249
Map	rs7953249
PheGenI	rs7953249
Biobank	rs7953249
1000 genomes	rs7953249
hgdp	rs7953249
ensembl	rs7953249
geneview	rs7953249
scholar	rs7953249
google	rs7953249
pharmgkb	rs7953249
gwascentral	rs7953249
openSNP	rs7953249
23andMe	rs7953249
SNPshot	rs7953249
SNPdbe	rs7953249
MSV3d	rs7953249
GWAS Ctlg	rs7953249

GMAF

0.427

Max Magnitude

0

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

GWAS snp
PMID	[PMID 21203500]
Trait
Title	Genomics Meets Glycomics-The First GWAS Study of Human N-Glycome Identifies HNF1± as a Master Regulator of Plasma Protein Fucosylation
Risk Allele	G
P-val	2E-8
Odds Ratio	0.1700 [0.11-0.23] unit decrease

[PMID 18439548] Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study.

[PMID 18940312] Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes.

GWAS snp
PMID	[PMID 23144326]
Trait	Chronic obstructive pulmonary disease-related biomarkers
Title	Genome-Wide Association Analysis of Blood Biomarkers in Chronic Obstructive Pulmonary Disease.
Risk Allele	G
P-val	1E-6
Odds Ratio	NR NR

[PMID 32100228] Associations Between Genomic Variants in lncRNA-TRPM2-AS and lncRNA-HNF1A-AS1 Genes and Risk of Multiple Sclerosis.