rs11193561

Orientation

plus

Stabilized

plus

Make rs11193561(C;C)

Make rs11193561(C;T)

Make rs11193561(T;T)

Reference

GRCh38 38.1/142

Chromosome

10

Position

107614626

is a	snp
is	mentioned by
dbSNP	rs11193561
dbSNP (classic)	rs11193561
ClinGen	rs11193561
ebi	rs11193561
HLI	rs11193561
Exac	rs11193561
Gnomad	rs11193561
Varsome	rs11193561
LitVar	rs11193561
Map	rs11193561
PheGenI	rs11193561
Biobank	rs11193561
1000 genomes	rs11193561
hgdp	rs11193561
ensembl	rs11193561
geneview	rs11193561
scholar	rs11193561
google	rs11193561
pharmgkb	rs11193561
gwascentral	rs11193561
openSNP	rs11193561
23andMe	rs11193561
SNPshot	rs11193561
SNPdbe	rs11193561
MSV3d	rs11193561
GWAS Ctlg	rs11193561

GMAF

0.2397

Max Magnitude

0

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

GWAS snp
PMID	[PMID 23472165]
Trait	Endometriosis
Title	Genome-wide association study link novel loci to endometriosis.
Risk Allele	A
P-val	6E-6
Odds Ratio	1.19 [NR]