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: rs2071591
rs2071591
0.925 0.160 6 31548022 intron variant G/A;C snv
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.700 1.000 1 2016 2016
dbSNP: rs2230365
rs2230365
0.925 0.160 6 31557671 synonymous variant C/T snv 0.16 0.13
CUI: C1629609
Disease: Age at menopause
Age at menopause
0.700 1.000 1 2015 2015
dbSNP: rs2857605
rs2857605
1.000 0.080 6 31557074 intron variant C/T snv 0.84
Diabetes Mellitus, Non-Insulin-Dependent
0.700 1.000 1 2018 2018
dbSNP: rs6929796
rs6929796
1.000 0.120 6 31554892 intron variant G/A snv 0.22
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs750884927
rs750884927
6 31555900 intron variant CC/-;C;CCC;CCCC delins
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2017 2017
dbSNP: rs9267488
rs9267488
1.000 0.080 6 31546470 splice region variant A/G snv 8.1E-02 9.9E-02
CUI: C0027121
Disease: Myositis
Myositis
0.700 1.000 1 2015 2015