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: rs2837828
rs2837828
21 40803034 intron variant A/G snv 0.44
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
0.800 1.000 1 2011 2011
dbSNP: rs727333
rs727333
1.000 0.080 21 40331020 intron variant C/A snv 6.6E-02
CUI: C0337434
Disease: Estradiol measurement
Estradiol measurement
0.800 1.000 1 2013 2013
dbSNP: rs727333
rs727333
1.000 0.080 21 40331020 intron variant C/A snv 6.6E-02
CUI: C1443016
Disease: Estradiol level result
Estradiol level result
0.800 1.000 1 2013 2013
dbSNP: rs2249498
rs2249498
1.000 0.080 21 40059947 intron variant T/A;C snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs2249498
rs2249498
1.000 0.080 21 40059947 intron variant T/A;C snv
Charcot-Marie-Tooth Disease, Type Ia (disorder)
0.700 1.000 1 2019 2019
dbSNP: rs2837398
rs2837398
21 40055241 intron variant A/C;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs2837554
rs2837554
1.000 0.080 21 40295451 intron variant A/G snv 0.78
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.700 1.000 1 2019 2019
dbSNP: rs3804024
rs3804024
21 40621781 intron variant T/C snv 9.0E-02
CUI: C2734068
Disease: Arm span
Arm span
0.700 1.000 1 2012 2012
dbSNP: rs455489
rs455489
21 40567642 intron variant A/C snv 0.15
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement
0.700 1.000 1 2019 2019
dbSNP: rs727333
rs727333
1.000 0.080 21 40331020 intron variant C/A snv 6.6E-02
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm
0.700 1.000 1 2019 2019
dbSNP: rs7282525
rs7282525
21 40088485 intron variant C/G;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs9980603
rs9980603
0.925 0.080 21 40514656 intron variant T/C snv 0.40
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.700 1.000 1 2013 2013
dbSNP: rs9980603
rs9980603
0.925 0.080 21 40514656 intron variant T/C snv 0.40
CUI: C0003467
Disease: Anxiety
Anxiety
0.700 1.000 1 2013 2013