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: 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: rs290986
rs290986
SYK
2 1.000 0.080 9 90801254 upstream gene variant A/G snv 0.18 0.800 1.000 2 2011 2016
dbSNP: rs307896
rs307896
SAE1
2 1.000 0.080 19 47158236 intron variant G/A;C snv 0.800 1.000 2 2011 2016
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: rs391745
rs391745 		3 0.925 0.080 X 97839482 intergenic variant C/G;T snv 0.020 0.500 2 2011 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: rs4285028
rs4285028
SLC15A2
2 1.000 0.080 3 121941817 3 prime UTR variant A/C;G snv 0.800 1.000 2 2011 2016
dbSNP: rs4410871
rs4410871
PVT1
2 0.925 0.080 8 127802783 intron variant T/C snv 0.74 0.800 1.000 2 2011 2013
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
dbSNP: rs630923
rs630923
CXCR5
2 1.000 0.080 11 118883644 upstream gene variant C/A snv 0.13 0.810 1.000 2 2011 2013
dbSNP: rs6680578
rs6680578
EVI5
1 1.000 0.080 1 92711321 intron variant T/A snv 0.57 0.020 1.000 2 2010 2017
dbSNP: rs669607
rs669607
LINC01967
1 1.000 0.080 3 28029953 intron variant A/C snv 0.38 0.800 1.000 2 2011 2016
dbSNP: rs6896969
rs6896969 		1 1.000 0.080 5 40424324 intron variant A/C;G snv 0.57 0.800 1.000 2 2009 2011
dbSNP: rs7382297
rs7382297
HLA-B
5 0.925 0.080 6 31279290 intron variant T/C;G snv 0.700 1.000 2 2007 2010
dbSNP: rs756699
rs756699 		1 1.000 0.080 5 134110884 upstream gene variant C/T snv 0.80 0.800 1.000 2 2011 2013
dbSNP: rs7595037
rs7595037 		1 1.000 0.080 2 68419963 regulatory region variant C/T snv 0.57 0.800 1.000 2 2011 2019
dbSNP: rs771767
rs771767 		2 1.000 0.080 3 102029794 regulatory region variant A/G snv 0.70 0.800 1.000 2 2011 2016
dbSNP: rs8042861
rs8042861
IQGAP1
1 1.000 0.080 15 90434101 intron variant G/A;T snv 0.710 1.000 2 2013 2016
dbSNP: rs9828519
rs9828519
SLC9A9
1 1.000 0.080 3 143707136 intron variant G/A;C;T snv 0.020 1.000 2 2015 2017
dbSNP: rs1014486
rs1014486
IL12A-AS1
1 1.000 0.080 3 159973324 intron variant T/C snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs1036207
rs1036207
NDFIP1
3 1.000 0.080 5 142119476 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10411936
rs10411936
EPS15L1
3 1.000 0.080 19 16437564 intron variant A/G snv 0.63 0.800 1.000 1 2011 2011
dbSNP: rs1044165
rs1044165
VSIG4
1 1.000 0.080 X 66021884 3 prime UTR variant G/A snv 9.0E-02 0.010 1.000 1 2015 2015
dbSNP: rs10466829
rs10466829
CLECL1
1 1.000 0.080 12 9723495 intron variant G/A snv 0.55 0.800 1.000 1 2011 2011