rs2648875

plus

Geno	Mag	Summary
(A;A)		8.82x increased risk of ESRD in diabetes type II patients
(A;G)		2.97x increased risk of ESRD in diabetes type II patients
(G;G)	0	normal

Reference

GRCh38 38.1/141

Chromosome

8

Position

128059915

Gene

PVT1

is a	snp
is	mentioned by
dbSNP	rs2648875
dbSNP (classic)	rs2648875
ClinGen	rs2648875
ebi	rs2648875
HLI	rs2648875
Exac	rs2648875
Gnomad	rs2648875
Varsome	rs2648875
LitVar	rs2648875
Map	rs2648875
PheGenI	rs2648875
Biobank	rs2648875
1000 genomes	rs2648875
hgdp	rs2648875
ensembl	rs2648875
geneview	rs2648875
scholar	rs2648875
google	rs2648875
pharmgkb	rs2648875
gwascentral	rs2648875
openSNP	rs2648875
23andMe	rs2648875
SNPshot	rs2648875
SNPdbe	rs2648875
MSV3d	rs2648875
GWAS Ctlg	rs2648875

GMAF

0.4132

Max Magnitude

0

?

(A;A) (A;G) (G;G)

28

Study of 105 unrelated case subjects with ESRD and 102 controls with type 2 diabetes for > or =10 years without macroalbuminuria. Association observed for rs2648875 (OR 2.97 per A allele) [1]

GWAS
SNP	rs2648875
PubMedID	[PMID 17395743]
Condition	End-stage renal disease
Gene	PVT1
Risk Allele	A
pValue	2.00E-006
OR	2.97
95% CI	1.90-4.65