Source: GWASCAT

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: 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 2 2011 2013
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: 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: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.710 1.000 3 2013 2017
dbSNP: rs10087240
rs10087240
PVT1
8 128000328 intron variant C/G;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs10087240
rs10087240
PVT1
8 128000328 intron variant C/G;T snv
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs10956401
rs10956401
PVT1
8 127990173 non coding transcript exon variant G/A snv 0.31
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs10956412
rs10956412
PVT1 ; MIR1208
1.000 0.040 8 128150251 intron variant A/C;G snv
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2019 2019
dbSNP: rs11786130
rs11786130
PVT1
8 127992729 intron variant G/A snv 0.31
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs11786130
rs11786130
PVT1
8 127992729 intron variant G/A snv 0.31
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs12156002
rs12156002
PVT1
1.000 0.080 8 128178298 intron variant C/A snv 0.24
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2017 2017
dbSNP: rs12548864
rs12548864
PVT1
8 127916000 intron variant C/T snv 0.27
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs12548939
rs12548939
PVT1 ; TMEM75
8 127946525 intron variant C/T snv 0.24
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs12548939
rs12548939
PVT1 ; TMEM75
8 127946525 intron variant C/T snv 0.24
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs12676304
rs12676304
PVT1
8 128151049 intron variant A/C snv 0.24
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs13254990
rs13254990
PVT1
0.882 0.120 8 128064205 intron variant C/T snv 0.24
CUI: C1334633
Disease: Mature B-Cell Neoplasm
Mature B-Cell Neoplasm 		0.700 1.000 1 2014 2014
dbSNP: rs13254990
rs13254990
PVT1
0.882 0.120 8 128064205 intron variant C/T snv 0.24
CUI: C2213246
Disease: Non-Hodgkin's lymphoma of central nervous system
Non-Hodgkin's lymphoma of central nervous system 		0.700 1.000 1 2019 2019
dbSNP: rs13255292
rs13255292
PVT1
0.925 0.120 8 128064327 intron variant C/T snv 0.24
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
Diffuse Large B-Cell Lymphoma 		0.700 1.000 1 2014 2014
dbSNP: rs13280095
rs13280095
PVT1
1.000 0.080 8 128166844 intron variant A/C snv 0.26
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2017 2017
dbSNP: rs1499364
rs1499364
PVT1
8 128167680 intron variant A/G snv 0.26
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs2608029
rs2608029
PVT1
1.000 0.040 8 128157880 intron variant C/G snv 0.37
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2019 2019
dbSNP: rs2608029
rs2608029
PVT1
1.000 0.040 8 128157880 intron variant C/G snv 0.37
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.700 1.000 1 2017 2017
dbSNP: rs2720680
rs2720680
PVT1
0.851 0.160 8 128102971 intron variant A/G snv 0.33
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		0.700 1.000 1 2017 2017