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: rs16942751
rs16942751
AQP4-AS1
1.000 0.080 18 26813249 intron variant C/A;T snv
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 4 2018 2019
dbSNP: rs1436904
rs1436904
CHST9 ; AQP4-AS1
0.851 0.080 18 26990703 intron variant T/G snv 0.35
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 3 2013 2017
dbSNP: rs527616
rs527616
AQP4-AS1
0.851 0.080 18 26757460 intron variant C/G snv 0.71
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 3 2013 2017
dbSNP: rs1154214
rs1154214
CHST9 ; AQP4-AS1
18 26966860 intron variant T/A;G snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs1186238
rs1186238
AQP4 ; AQP4-AS1
18 26857540 intron variant A/C snv
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2018 2018
dbSNP: rs12458099
rs12458099
CHST9 ; AQP4-AS1
1.000 0.080 18 27025475 intron variant G/A;T snv 0.38
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs151246
rs151246
AQP4-AS1
18 26869139 intron variant T/G snv 0.77
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2018 2018
dbSNP: rs151246
rs151246
AQP4-AS1
18 26869139 intron variant T/G snv 0.77
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2018 2018
dbSNP: rs162005
rs162005
AQP4-AS1
18 26867822 intron variant G/A snv 0.78
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs16942713
rs16942713
AQP4-AS1
18 26806571 intron variant G/T snv 0.10
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		0.700 1.000 1 2019 2019
dbSNP: rs16942751
rs16942751
AQP4-AS1
1.000 0.080 18 26813249 intron variant C/A;T snv
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2018 2018
dbSNP: rs16942751
rs16942751
AQP4-AS1
1.000 0.080 18 26813249 intron variant C/A;T snv
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		0.700 1.000 1 2019 2019
dbSNP: rs16942981
rs16942981
CHST9 ; AQP4-AS1
0.925 0.040 18 26937284 intron variant T/C snv 0.12
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs16942981
rs16942981
CHST9 ; AQP4-AS1
0.925 0.040 18 26937284 intron variant T/C snv 0.12
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs2307561
rs2307561
CHST9 ; AQP4-AS1
1.000 0.080 18 26923543 intron variant AGTGTT/- del 0.28
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs528732638
rs528732638
CHST9 ; AQP4-AS1
0.851 0.120 18 26940224 intron variant A/-;AA;AAA;AAAA delins
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs528732638
rs528732638
CHST9 ; AQP4-AS1
0.851 0.120 18 26940224 intron variant A/-;AA;AAA;AAAA delins
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
dbSNP: rs7233634
rs7233634
CHST9 ; AQP4-AS1
18 27137739 intron variant T/C snv 0.32
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs9952639
rs9952639
CHST9 ; AQP4-AS1
18 27129640 intron variant G/C snv 0.32
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs9953924
rs9953924
AQP4-AS1 ; LOC102725227
18 26680575 intron variant C/G snv 0.92
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019