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: rs1399439
rs1399439
ANO4
1.000 0.080 12 100827461 intron variant A/G snv 3.7E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.800 1.000 1 2014 2014
dbSNP: rs118152513
rs118152513
ANO4
12 100790474 intron variant T/C snv 2.1E-03
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs183825572
rs183825572
ANO4
12 100871067 intron variant G/A snv 1.8E-04
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs188024766
rs188024766
ANO4
12 100959756 intron variant C/G snv 3.6E-04
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs2138050
rs2138050
ANO4
0.925 0.040 12 100886729 intron variant C/G;T snv 0.33
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs2138050
rs2138050
ANO4
0.925 0.040 12 100886729 intron variant C/G;T snv 0.33
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs644939
rs644939
ANO4
1.000 0.040 12 101060211 intron variant G/A snv 0.24
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017
dbSNP: rs686288
rs686288
ANO4
12 100982873 intron variant A/G snv 4.6E-02
CUI: C0201899
Disease: Aspartate aminotransferase measurement
Aspartate aminotransferase measurement 		0.700 1.000 1 2019 2019