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: rs17824933
rs17824933
CD6
1 1.000 0.080 11 60993140 intron variant C/A;G snv 0.850 1.000 7 2009 2016
dbSNP: rs1335532
rs1335532
CD58
1 1.000 0.080 1 116558335 intron variant A/G snv 0.28 0.810 1.000 5 2009 2018
dbSNP: rs10492972
rs10492972
KIF1B
1 1.000 0.080 1 10293054 intron variant T/C snv 0.32 0.830 1.000 4 2008 2011
dbSNP: rs12368653
rs12368653
TSPAN31 ; AGAP2
1 1.000 0.080 12 57739473 intron variant G/A;T snv 0.820 1.000 4 2009 2018
dbSNP: rs180515
rs180515
RPS6KB1
1 1.000 0.080 17 59946914 3 prime UTR variant A/G snv 0.33 0.820 1.000 3 2011 2017
dbSNP: rs9282641
rs9282641
CD86
1 1.000 0.080 3 122077921 splice region variant G/A snv 7.0E-02 0.820 1.000 3 2011 2018
dbSNP: rs10201872
rs10201872
SP140
1 1.000 0.080 2 230242009 intron variant C/T snv 0.13 0.810 1.000 2 2011 2015
dbSNP: rs1021156
rs1021156
LOC105375911
1 1.000 0.080 8 78663569 intron variant T/C snv 0.64 0.710 1.000 2 2013 2016
dbSNP: rs10735781
rs10735781
EVI5
1 1.000 0.080 1 92655550 intron variant G/C snv 0.57 0.710 1.000 2 2011 2017
dbSNP: rs11129295
rs11129295 		1 1.000 0.080 3 27747289 intergenic variant C/T snv 0.39 0.810 1.000 2 2011 2018
dbSNP: rs11567685
rs11567685
IL7R ; LOC105374724
1 1.000 0.080 5 35856473 5 prime UTR variant T/C snv 0.26 0.020 < 0.001 2 2014 2017
dbSNP: rs11808092
rs11808092
EVI5
1 1.000 0.080 1 92607671 missense variant C/A snv 0.20 0.20 0.710 1.000 2 2010 2016
dbSNP: rs11810217
rs11810217
EVI5
1 1.000 0.080 1 92682820 intron variant C/T snv 0.20 0.810 1.000 2 2011 2017
dbSNP: rs12025416
rs12025416
LOC112268235
1 1.000 0.080 1 116495665 intron variant T/A;C snv 0.800 1.000 2 2009 2011
dbSNP: rs1841770
rs1841770 		1 1.000 0.080 3 148038899 intron variant G/T snv 0.64 0.020 1.000 2 2011 2012
dbSNP: rs2068330
rs2068330
KCNH7
1 1.000 0.080 2 162380880 intron variant C/G snv 0.49 0.020 1.000 2 2008 2009
dbSNP: rs2255214
rs2255214
ILDR1
1 1.000 0.080 3 122051692 upstream gene variant G/T snv 0.44 0.700 1.000 2 2013 2016
dbSNP: rs2283792
rs2283792
MAPK1
1 1.000 0.080 22 21776836 intron variant T/G snv 0.54 0.800 1.000 2 2011 2013
dbSNP: rs243324
rs243324
RMI2 ; LOC105371082
1 1.000 0.080 16 11261113 intron variant A/G snv 0.51 0.020 0.500 2 2012 2015
dbSNP: rs2681424
rs2681424
ILDR1
1 1.000 0.080 3 122050675 upstream gene variant T/A;C snv 0.800 1.000 2 2011 2016
dbSNP: rs2744148
rs2744148 		1 1.000 0.080 16 1023552 intergenic variant A/G snv 0.15 0.810 1.000 2 2011 2013
dbSNP: rs2836425
rs2836425
ERG
1 1.000 0.080 21 38466902 intron variant C/T snv 0.11 0.710 1.000 2 2016 2019
dbSNP: rs34286592
rs34286592
MAZ ; LOC112268170
1 1.000 0.080 16 29809159 intron variant C/T snv 0.12 0.710 0.500 2 2016 2019
dbSNP: rs397020
rs397020
RAD21L1
1 1.000 0.080 20 1225242 upstream gene variant T/A;C snv 0.810 1.000 2 2009 2011
dbSNP: rs4925166
rs4925166
TOP3A
1 1.000 0.080 17 18307496 3 prime UTR variant T/G snv 0.45 0.73 0.710 1.000 2 2016 2019