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: rs10623258
rs10623258
ADSS1
1.000 0.080 14 104745924 non coding transcript exon variant -/TT ins 0.56
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs10647170
rs10647170
PRMT3
11 20410500 intron variant -/GGTC;GTTC;TGTC ins
CUI: C3548532
Disease: response to alcohol
response to alcohol 		0.700 1.000 1 2020 2020
dbSNP: rs10674174
rs10674174 		1.000 0.120 13 61317942 intergenic variant -/G ins
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		0.700 1.000 1 2016 2016
dbSNP: rs112925537
rs112925537
INO80
15 41042015 intron variant -/C ins
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2017 2017
dbSNP: rs112925537
rs112925537
INO80
15 41042015 intron variant -/C ins
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2017 2017
dbSNP: rs113309773
rs113309773
CFDP1
1.000 0.080 16 75398788 intron variant -/A;C ins 0.51
CUI: C0577631
Disease: Carotid Atherosclerosis
Carotid Atherosclerosis 		0.700 1.000 1 2018 2018
dbSNP: rs113352172
rs113352172
PDCD1LG2
9 5510837 intron variant -/G;GTTTATGTTGAGATACTCTCATACTG ins 0.26
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs11374964
rs11374964
POGLUT3
1.000 0.080 11 108474788 3 prime UTR variant -/A ins 2.4E-05; 0.47 0.43
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs11377084
rs11377084
LINC01169
15 66651883 intron variant -/A ins 0.67
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs11391380
rs11391380 		3 105336694 intergenic variant -/G ins 0.66
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs11412402
rs11412402
EEFSEC
0.925 0.080 3 128194003 intron variant -/T ins 0.65
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
dbSNP: rs11412402
rs11412402
EEFSEC
0.925 0.080 3 128194003 intron variant -/T ins 0.65
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		0.700 1.000 1 2019 2019
dbSNP: rs11428934
rs11428934
CA11 ; SEC1P
19 48640988 intron variant -/G ins
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs11428934
rs11428934
CA11 ; SEC1P
19 48640988 intron variant -/G ins
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs11428934
rs11428934
CA11 ; SEC1P
19 48640988 intron variant -/G ins
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs11428934
rs11428934
CA11 ; SEC1P
19 48640988 intron variant -/G ins
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs11438927
rs11438927 		12 120746070 intron variant -/C ins 0.42
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs11451044
rs11451044
COPZ1
12 54322000 intron variant -/A ins 0.68
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs11454451
rs11454451
GPATCH2
1 217549548 intron variant -/T ins 0.23
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE 		0.700 1.000 1 2016 2016
dbSNP: rs11471957
rs11471957
TUBB1
20 59023277 intron variant -/AA ins
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs11471957
rs11471957
TUBB1
20 59023277 intron variant -/AA ins
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs141424017
rs141424017 		1.000 0.080 7 115311376 intergenic variant -/CAA ins
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		0.700 1.000 1 2019 2019
dbSNP: rs141424017
rs141424017 		1.000 0.080 7 115311376 intergenic variant -/CAA ins
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		0.700 1.000 1 2019 2019
dbSNP: rs141424017
rs141424017 		1.000 0.080 7 115311376 intergenic variant -/CAA ins
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		0.700 1.000 1 2019 2019
dbSNP: rs145013566
rs145013566
PNKD
2 218297998 intron variant -/C ins
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016