Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2019960
rs2019960
PVT1
0.925 0.160 8 128180025 intron variant T/C snv 0.27
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		0.800 1.000 3 2010 2014
dbSNP: rs2019960
rs2019960
PVT1
0.925 0.160 8 128180025 intron variant T/C snv 0.27
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.800 1.000 1 2011 2011
dbSNP: rs2608053
rs2608053
PVT1
1.000 0.120 8 128063586 intron variant T/C snv 0.50
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		0.800 1.000 1 2010 2010
dbSNP: rs4410871
rs4410871
PVT1
0.925 0.080 8 127802783 intron variant T/C snv 0.74
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.800 1.000 1 2011 2013
dbSNP: rs6470588
rs6470588
PVT1
1.000 0.120 8 127877125 intron variant A/C snv 0.53
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		0.800 1.000 1 2013 2013
dbSNP: rs11780156
rs11780156
PVT1
0.925 0.080 8 128182395 intron variant C/T snv 0.13
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.710 1.000 1 2013 2016
dbSNP: rs13255292
rs13255292
PVT1
0.925 0.120 8 128064327 intron variant C/T snv 0.24
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		0.700 1.000 1 2013 2013
dbSNP: rs4410871
rs4410871
PVT1
0.925 0.080 8 127802783 intron variant T/C snv 0.74
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization 		0.700 1.000 1 2013 2013
dbSNP: rs4733809
rs4733809
PVT1
1.000 0.120 8 127977046 intron variant C/T snv 0.54
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		0.700 1.000 1 2013 2013
dbSNP: rs752427
rs752427
PVT1
1.000 0.120 8 127967762 intron variant C/T snv 0.55
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		0.700 1.000 1 2013 2013