Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1047972
rs1047972
AURKA
19 0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 0.010 1.000 1 2015 2015
dbSNP: rs11075995
rs11075995
FTO
5 0.882 0.080 16 53821379 intron variant A/T snv 0.77 0.010 1.000 1 2014 2014
dbSNP: rs121909222
rs121909222
PTEN
13 0.742 0.240 10 87933127 missense variant A/G snv 0.010 1.000 1 2016 2016
dbSNP: rs12493607
rs12493607
TGFBR2
3 0.882 0.080 3 30641447 intron variant G/C;T snv 0.010 1.000 1 2014 2014
dbSNP: rs2070235
rs2070235
MYBL2
1 1.000 20 43702817 missense variant A/G snv 0.10 0.14 0.010 1.000 1 2009 2009
dbSNP: rs3104746
rs3104746
CASC16
7 0.790 0.120 16 52567188 intron variant T/A snv 8.6E-02 0.010 1.000 1 2014 2014
dbSNP: rs6099128
rs6099128
AURKA
2 0.925 20 56390288 intron variant T/G snv 0.13 0.010 1.000 1 2015 2015
dbSNP: rs9436746
rs9436746
LEPR
1 1.000 1 65442790 intron variant A/C snv 0.50 0.010 < 0.001 1 2011 2011
dbSNP: rs9436748
rs9436748
LEPR
1 1.000 1 65445989 intron variant G/A;T snv 0.33 0.010 < 0.001 1 2011 2011