rs2066807

minus

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

Make rs2066807(C;C)

Make rs2066807(C;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

56346898

Gene

STAT2

is a	snp
is	mentioned by
dbSNP	rs2066807
dbSNP (classic)	rs2066807
ClinGen	rs2066807
ebi	rs2066807
HLI	rs2066807
Exac	rs2066807
Gnomad	rs2066807
Varsome	rs2066807
LitVar	rs2066807
Map	rs2066807
PheGenI	rs2066807
Biobank	rs2066807
1000 genomes	rs2066807
hgdp	rs2066807
ensembl	rs2066807
geneview	rs2066807
scholar	rs2066807
google	rs2066807
pharmgkb	rs2066807
gwascentral	rs2066807
openSNP	rs2066807
23andMe	rs2066807
SNPshot	rs2066807
SNPdbe	rs2066807
MSV3d	rs2066807
GWAS Ctlg	rs2066807

GMAF

0.04591

Max Magnitude

0

?

(C;C) (C;G) (G;G)

28

GWAS snp
PMID	[PMID 20881960 ]
Trait	Height
Title	Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele	C
P-val	1E-13
Odds Ratio	.05 [NR] unit decrease

[PMID 19159017 ] STAT2*C related genotypes and allele but not TLR4 and CD40 gene polymorphisms are associated with higher susceptibility for asthma.

[PMID 19169254 ] Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways.

[PMID 19434718 ] Variants in interferon-alpha pathway genes and response to pegylated interferon-Alpha2a plus ribavirin for treatment of chronic hepatitis C virus infection in the hepatitis C antiviral long-term treatment against cirrhosis trial.

[PMID 21499878] Association of toll-like receptor 9 gene polymorphism in Chinese patients with systemic lupus erythematosus in Taiwan.

ClinVar
Risk	rs2066807(C;C)
Alt	rs2066807(C;C)
Reference	Rs2066807(G;G)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	STAT2
CLNDBN	not specified
Reversed	1
HGVS	NC_000012.11:g.56740682C>G
CLNSRC
CLNACC	RCV000455792.1,