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: rs10988217
rs10988217
PTPA
1 1.000 0.080 9 129125837 intron variant A/G snv 0.45 0.700 1.000 1 2018 2018
dbSNP: rs16826005
rs16826005
NCKAP5
1 1.000 0.080 2 133508430 intron variant A/G snv 7.4E-02 0.700 1.000 1 2013 2013
dbSNP: rs16966389
rs16966389 		1 1.000 0.080 15 38172673 intron variant G/A snv 3.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs359268
rs359268 		1 1.000 0.080 2 60232671 intergenic variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs7725217
rs7725217
LINC02112 ; LOC105374649
1 1.000 0.080 5 9756217 intron variant A/C snv 0.25 0.700 1.000 1 2013 2013
dbSNP: rs2119882
rs2119882
MTNR1A
9 0.807 0.320 4 186555751 upstream gene variant T/C snv 0.57 0.010 1.000 1 2011 2011
dbSNP: rs4680
rs4680
COMT ; MIR4761
249 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 0.010 1.000 1 2017 2017