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: rs9376092
rs9376092
LOC105378010
10 0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 0.020 1.000 2 2015 2017
dbSNP: rs780178275
rs780178275
VHL
7 0.851 0.200 3 10146586 missense variant C/T snv 8.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs777342222
rs777342222
EGFR
1 1.000 0.080 7 55155925 missense variant T/C snv 4.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs775387828
rs775387828
NFE2
7 0.851 0.200 12 54293083 missense variant G/A snv 2.2E-05 7.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs77375493
rs77375493
JAK2 ; INSL6
187 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.900 0.960 274 2005 2019
dbSNP: rs773475680
rs773475680
ABL1
1 1.000 0.080 9 130884139 missense variant C/T snv 4.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs772889171
rs772889171
RUNX1
2 0.925 0.080 21 34834487 missense variant G/A snv 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs766642690
rs766642690
MPL
1 1.000 0.080 1 43352635 missense variant T/C;G snv 4.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs754190776
rs754190776
HBG2
2 0.925 0.080 11 5253350 missense variant G/A snv 8.0E-06 0.010 1.000 1 1989 1989
dbSNP: rs7046736
rs7046736
JAK2 ; INSL6
2 0.925 0.080 9 5015732 intron variant C/A snv 0.39 0.010 1.000 1 2008 2008
dbSNP: rs562533120
rs562533120
HBS1L
3 0.882 0.080 6 134966397 missense variant A/C snv 8.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs4495487
rs4495487
JAK2 ; INSL6
3 0.925 0.080 9 5072798 intron variant T/C snv 0.23 0.010 1.000 1 2012 2012
dbSNP: rs4073
rs4073
CXCL8
64 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2019 2019
dbSNP: rs397507444
rs397507444
MTHFR
306 0.405 0.880 1 11794407 missense variant T/G snv 0.010 1.000 1 2014 2014
dbSNP: rs3808850
rs3808850
JAK2
2 0.925 0.080 9 4983311 upstream gene variant T/A;C snv 0.010 1.000 1 2008 2008
dbSNP: rs361525
rs361525
TNF
62 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2019 2019
dbSNP: rs318699
rs318699
RGL3
3 0.882 0.080 19 11390564 intron variant A/G snv 0.73 0.010 1.000 1 2008 2008
dbSNP: rs2736100
rs2736100
TERT
83 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 0.030 1.000 3 2015 2018
dbSNP: rs267606870
rs267606870
IDH2
11 0.763 0.280 15 90088703 missense variant G/A;C snv 0.010 1.000 1 2010 2010
dbSNP: rs2201862
rs2201862 		3 0.925 0.080 3 168930251 downstream gene variant T/C snv 0.63 0.010 1.000 1 2017 2017
dbSNP: rs201478192
rs201478192
KIDINS220
12 0.790 0.200 2 8731667 missense variant C/A snv 2.4E-04 2.6E-04 0.040 1.000 4 2013 2015
dbSNP: rs17849241
rs17849241
SOCS3 ; LOC101928674
3 0.925 0.080 17 78358688 missense variant G/C;T snv 4.1E-06; 2.1E-04 0.010 1.000 1 2009 2009
dbSNP: rs17576
rs17576
MMP9
73 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.010 < 0.001 1 2015 2015
dbSNP: rs12979860
rs12979860
IFNL4
84 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2018 2018
dbSNP: rs1253570532
rs1253570532
RUNX1
2 0.925 0.080 21 34792289 missense variant G/A snv 7.0E-06 0.010 1.000 1 2013 2013