rs2400997

Orientation

plus

Stabilized

plus

Make rs2400997(C;C)

Make rs2400997(C;T)

Make rs2400997(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

101260770

is a	snp
is	mentioned by
dbSNP	rs2400997
dbSNP (classic)	rs2400997
ClinGen	rs2400997
ebi	rs2400997
HLI	rs2400997
Exac	rs2400997
Gnomad	rs2400997
Varsome	rs2400997
LitVar	rs2400997
Map	rs2400997
PheGenI	rs2400997
Biobank	rs2400997
1000 genomes	rs2400997
hgdp	rs2400997
ensembl	rs2400997
geneview	rs2400997
scholar	rs2400997
google	rs2400997
pharmgkb	rs2400997
gwascentral	rs2400997
openSNP	rs2400997
23andMe	rs2400997
SNPshot	rs2400997
SNPdbe	rs2400997
MSV3d	rs2400997
GWAS Ctlg	rs2400997

GMAF

0.3659

Max Magnitude

0

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

GWAS snp
PMID	[PMID 22219177]
Trait
Title	A genome-wide search for loci interacting with known prostate cancer risk-associated genetic variants.
Risk Allele
P-val	0.000003
Odds Ratio	1.2500 None