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: rs2923084
rs2923084
AMPD3 ; CAND1.11
11 10367235 intron variant A/G snv 0.29
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 2 2010 2013
dbSNP: rs6484218
rs6484218
AMPD3 ; CAND1.11
0.882 0.040 11 10369034 intron variant G/A snv 0.21
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders 		0.800 1.000 1 2010 2010
dbSNP: rs6484218
rs6484218
AMPD3 ; CAND1.11
0.882 0.040 11 10369034 intron variant G/A snv 0.21
CUI: C0004936
Disease: Mental disorders
Mental disorders 		0.800 1.000 1 2010 2010
dbSNP: rs7129220
rs7129220
AMPD3 ; CAND1.11
11 10328991 intron variant G/A snv 0.10
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 2 2011 2017
dbSNP: rs7129220
rs7129220
AMPD3 ; CAND1.11
11 10328991 intron variant G/A snv 0.10
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 2 2011 2017
dbSNP: rs10770117
rs10770117
AMPD3 ; CAND1.11
11 10426370 intron variant T/C snv 0.29
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs11042841
rs11042841
AMPD3
11 10483662 intron variant C/G snv 0.70
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs1450271
rs1450271
AMPD3 ; CAND1.11
11 10334568 intron variant C/T snv 0.43
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2016 2016
dbSNP: rs1450271
rs1450271
AMPD3 ; CAND1.11
11 10334568 intron variant C/T snv 0.43
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2016 2016
dbSNP: rs1562782
rs1562782
AMPD3 ; CAND1.11
11 10321164 intron variant A/C;G snv
CUI: C0429097
Disease: QRS complex feature
QRS complex feature 		0.700 1.000 1 2016 2016
dbSNP: rs2084600
rs2084600
AMPD3 ; CAND1.11
11 10330748 intron variant A/G snv 0.41
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs2860284
rs2860284
AMPD3 ; CAND1.11
11 10364929 intron variant T/C snv 0.73
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs2923097
rs2923097
AMPD3 ; CAND1.11
11 10343497 intron variant A/G;T snv
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2019 2019
dbSNP: rs2957658
rs2957658
AMPD3 ; CAND1.11
11 10371921 intron variant G/A snv 0.45
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs4444073
rs4444073
AMPD3 ; CAND1.11
11 10310117 intron variant A/C snv 0.38
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2019 2019
dbSNP: rs6484218
rs6484218
AMPD3 ; CAND1.11
0.882 0.040 11 10369034 intron variant G/A snv 0.21
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 1.000 1 2010 2010
dbSNP: rs6484218
rs6484218
AMPD3 ; CAND1.11
0.882 0.040 11 10369034 intron variant G/A snv 0.21
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2010 2010
dbSNP: rs72856182
rs72856182
AMPD3
11 10444927 intron variant T/C snv 0.18
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs899013
rs899013
AMPD3
11 10455142 intron variant A/G snv 0.60
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019