rs9977499

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;T)	0	common in complete genomics

Make rs9977499(C;C)

Make rs9977499(T;T)

Reference

GRCh38 38.1/141

Chromosome

21

Position

27362678

is a	snp
is	mentioned by
dbSNP	rs9977499
dbSNP (classic)	rs9977499
ClinGen	rs9977499
ebi	rs9977499
HLI	rs9977499
Exac	rs9977499
Gnomad	rs9977499
Varsome	rs9977499
LitVar	rs9977499
Map	rs9977499
PheGenI	rs9977499
Biobank	rs9977499
1000 genomes	rs9977499
hgdp	rs9977499
ensembl	rs9977499
geneview	rs9977499
scholar	rs9977499
google	rs9977499
pharmgkb	rs9977499
gwascentral	rs9977499
openSNP	rs9977499
23andMe	rs9977499
SNPshot	rs9977499
SNPdbe	rs9977499
MSV3d	rs9977499
GWAS Ctlg	rs9977499

GMAF

0.3788

Max Magnitude

0

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

GWAS snp
PMID	[PMID 21546767]
Trait
Title	Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes.
Risk Allele
P-val	0.000004
Odds Ratio	1.5700 [1.29-1.91]