rs12615966

Orientation

plus

Stabilized

plus

Make rs12615966(C;C)

Make rs12615966(C;T)

Make rs12615966(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

104762499

is a	snp
is	mentioned by
dbSNP	rs12615966
dbSNP (classic)	rs12615966
ClinGen	rs12615966
ebi	rs12615966
HLI	rs12615966
Exac	rs12615966
Gnomad	rs12615966
Varsome	rs12615966
LitVar	rs12615966
Map	rs12615966
PheGenI	rs12615966
Biobank	rs12615966
1000 genomes	rs12615966
hgdp	rs12615966
ensembl	rs12615966
geneview	rs12615966
scholar	rs12615966
google	rs12615966
pharmgkb	rs12615966
gwascentral	rs12615966
openSNP	rs12615966
23andMe	rs12615966
SNPshot	rs12615966
SNPdbe	rs12615966
MSV3d	rs12615966
GWAS Ctlg	rs12615966

GMAF

0.1309

Max Magnitude

0

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

GWAS snp
PMID	[PMID 20686608]
Trait
Title	Genome-wide association study of pancreatic cancer in Japanese population
Risk Allele	A
P-val	0.000007
Odds Ratio	3.15 [1.91-5.21]