Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10119
rs10119
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
Mental Disorders 0.010 < 0.001 1 2011 2011
dbSNP: rs11556510
rs11556510
1.000 0.040 19 44891562 missense variant T/G snv 9.8E-03 1.2E-02
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
Mental Disorders 0.010 < 0.001 1 2011 2011
dbSNP: rs157581
rs157581
0.925 0.080 19 44892457 synonymous variant T/C snv 0.25 0.29
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs2075650
rs2075650
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs59007384
rs59007384
0.851 0.080 19 44893408 intron variant G/A;T snv
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
Mental Disorders 0.010 < 0.001 1 2011 2011