rs17391694

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0

Make rs17391694(C;T)

Make rs17391694(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

78157942

is a	snp
is	mentioned by
dbSNP	rs17391694
dbSNP (classic)	rs17391694
ClinGen	rs17391694
ebi	rs17391694
HLI	rs17391694
Exac	rs17391694
Gnomad	rs17391694
Varsome	rs17391694
LitVar	rs17391694
Map	rs17391694
PheGenI	rs17391694
Biobank	rs17391694
1000 genomes	rs17391694
hgdp	rs17391694
ensembl	rs17391694
geneview	rs17391694
scholar	rs17391694
google	rs17391694
pharmgkb	rs17391694
gwascentral	rs17391694
openSNP	rs17391694
23andMe	rs17391694
SNPshot	rs17391694
SNPdbe	rs17391694
MSV3d	rs17391694
GWAS Ctlg	rs17391694

GMAF

0.04362

Max Magnitude

0

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

GWAS snp
PMID	[PMID 20881960]
Trait
Title	Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele	T
P-val	2E-11
Odds Ratio	0.0400 [NR] meters increase

GWAS snp
PMID	[PMID 23128233]
Trait	Crohn's disease
Title	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Risk Allele	C
P-val	3E-9
Odds Ratio	1.13 [1.077-1.194]