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: rs6478241
rs6478241
ASTN2
0.925 0.040 9 116490350 intron variant A/G;T snv
CUI: C0338480
Disease: Common Migraine
Common Migraine 		0.810 1.000 1 2013 2016
dbSNP: rs6478241
rs6478241
ASTN2
0.925 0.040 9 116490350 intron variant A/G;T snv
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		0.800 1.000 3 2012 2016
dbSNP: rs10983238
rs10983238
ASTN2 ; LOC107987015
1.000 0.040 9 116571404 intron variant C/A;G snv 0.16
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.800 1.000 1 2008 2008
dbSNP: rs13290997
rs13290997
ASTN2 ; ASTN2-AS1
9 116551938 intron variant A/G snv 0.58
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.800 1.000 1 2012 2012
dbSNP: rs13283416
rs13283416
ASTN2 ; ASTN2-AS1
1.000 0.040 9 116539328 intron variant T/G snv 0.41
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 2 2019 2019
dbSNP: rs4836732
rs4836732
ASTN2 ; ASTN2-AS1
1.000 0.040 9 116504416 intron variant C/T snv 0.49
CUI: C0029410
Disease: Osteoarthritis of hip
Osteoarthritis of hip 		0.700 1.000 2 2018 2019
dbSNP: rs10817888
rs10817888
ASTN2
9 116428254 intron variant G/A snv 0.32
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10817898
rs10817898
ASTN2
9 116492446 intron variant C/T snv 0.51
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs10817969
rs10817969
ASTN2
1.000 0.040 9 116968766 intron variant T/C;G snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2019 2019
dbSNP: rs10983184
rs10983184
ASTN2
9 116471779 intron variant C/T snv 0.55
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2019 2019
dbSNP: rs10983184
rs10983184
ASTN2
9 116471779 intron variant C/T snv 0.55
CUI: C1518922
Disease: peak expiratory flow (procedure)
peak expiratory flow (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs10983324
rs10983324
ASTN2
9 116723058 intron variant C/A;G;T snv
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs10983614
rs10983614
ASTN2
1.000 0.120 9 117306874 intron variant T/A;C snv
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs117491755
rs117491755
ASTN2
1.000 0.080 9 116881377 intron variant A/C snv 2.6E-02
CUI: C4277682
Disease: Chemical and Drug Induced Liver Injury
Chemical and Drug Induced Liver Injury 		0.700 1.000 1 2017 2017
dbSNP: rs1321917
rs1321917
ASTN2 ; ASTN2-AS1
9 116562650 intron variant G/A;C snv
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs13283416
rs13283416
ASTN2 ; ASTN2-AS1
1.000 0.040 9 116539328 intron variant T/G snv 0.41
CUI: C0029410
Disease: Osteoarthritis of hip
Osteoarthritis of hip 		0.700 1.000 1 2018 2018
dbSNP: rs13290997
rs13290997
ASTN2 ; ASTN2-AS1
9 116551938 intron variant A/G snv 0.58
CUI: C0035227
Disease: Respiratory Function Tests
Respiratory Function Tests 		0.700 1.000 1 2012 2012
dbSNP: rs13298297
rs13298297
ASTN2
9 116501829 intron variant G/A snv 0.21
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2017 2017
dbSNP: rs13298297
rs13298297
ASTN2
9 116501829 intron variant G/A snv 0.21
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2017 2017
dbSNP: rs1335415
rs1335415
ASTN2 ; LOC105376237
0.925 0.040 9 117254067 intron variant C/A;T snv 0.22
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs1335415
rs1335415
ASTN2 ; LOC105376237
0.925 0.040 9 117254067 intron variant C/A;T snv 0.22
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs1372330
rs1372330
ASTN2
1.000 0.080 9 116757309 intron variant G/A snv 0.13
CUI: C4721579
Disease: Secondary malignant neoplasm of colon and/or rectum
Secondary malignant neoplasm of colon and/or rectum 		0.700 1.000 1 2019 2019
dbSNP: rs17220352
rs17220352
ASTN2
9 116485780 intron variant A/G snv 0.21
CUI: C0018681
Disease: Headache
Headache 		0.700 1.000 1 2018 2018
dbSNP: rs1861881
rs1861881
ASTN2 ; ASTN2-AS1
9 116549977 intron variant G/A;T snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs1895062
rs1895062
ASTN2 ; ASTN2-AS1
1.000 0.080 9 116551207 intron variant A/G snv 0.32
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2017 2017