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: rs1135401746
rs1135401746
GNB1
7 0.827 0.400 1 1806512 missense variant C/G snv 0.700 0
dbSNP: rs121909646
rs121909646
FLT3
3 0.882 0.120 13 28018504 missense variant T/A;G snv 0.700 0
dbSNP: rs121913232
rs121913232
FLT3
2 0.925 0.120 13 28018500 missense variant G/C snv 0.700 0
dbSNP: rs121913487
rs121913487
FLT3
2 0.925 0.120 13 28018503 missense variant A/C;T snv 0.700 0
dbSNP: rs121913488
rs121913488
FLT3
7 0.807 0.120 13 28018505 missense variant C/A;G;T snv 0.700 0
dbSNP: rs1478147351
rs1478147351
SETD2
1 1.000 0.120 3 47101485 missense variant G/A snv 7.0E-06 0.700 0
dbSNP: rs186148199
rs186148199
SETD2
1 1.000 0.120 3 47123837 missense variant C/T snv 8.9E-05 3.5E-05 0.700 0
dbSNP: rs188887061
rs188887061
SETD2
1 1.000 0.120 3 47122353 missense variant C/T snv 4.2E-04 7.0E-05 0.700 0
dbSNP: rs398123063
rs398123063
PAX5 ; LOC105376032
2 0.925 0.120 9 37002705 missense variant C/T snv 0.700 0
dbSNP: rs11155133
rs11155133
LOC102723724
2 0.925 0.200 6 140848688 intron variant A/G snv 8.5E-02 0.800 1.000 1 2009 2009
dbSNP: rs17079534
rs17079534 		1 1.000 0.120 3 39805581 upstream gene variant G/A;C snv 0.800 1.000 1 2012 2012
dbSNP: rs17505102
rs17505102
TP63
1 1.000 0.120 3 189683987 intron variant G/C snv 9.7E-02 0.800 1.000 1 2012 2012
dbSNP: rs1945213
rs1945213 		1 1.000 0.120 11 56408195 upstream gene variant C/G;T snv 0.800 1.000 1 2012 2012
dbSNP: rs207954
rs207954
SLCO3A1
1 1.000 0.120 15 92114143 intron variant T/A;C;G snv 0.800 1.000 1 2012 2012
dbSNP: rs2089222
rs2089222
MAP1LC3B2
2 0.925 0.200 12 116564853 intron variant G/A snv 0.12 0.800 1.000 1 2009 2009
dbSNP: rs2191566
rs2191566
ZNF230
2 0.925 0.200 19 44007237 intron variant G/T snv 0.62 0.800 1.000 1 2009 2009
dbSNP: rs3942852
rs3942852
PTPRJ
1 1.000 0.120 11 48093537 intron variant C/T snv 0.69 0.800 1.000 1 2012 2012
dbSNP: rs4982731
rs4982731 		1 1.000 0.120 14 23116124 downstream gene variant C/T snv 0.68 0.800 1.000 1 2013 2013
dbSNP: rs6964969
rs6964969
IKZF1
4 0.851 0.120 7 50405553 downstream gene variant A/G snv 0.23 0.800 1.000 1 2013 2013
dbSNP: rs7142143
rs7142143
PYGL
1 1.000 0.120 14 50936813 intron variant T/C snv 2.8E-02 0.800 1.000 1 2012 2012
dbSNP: rs7156960
rs7156960
GPATCH2L ; LOC105370575
1 1.000 0.120 14 76237008 intron variant C/G;T snv 0.800 1.000 1 2012 2012
dbSNP: rs10261922
rs10261922 		1 1.000 0.120 7 50414314 intergenic variant C/A;G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1037351
rs1037351
DDC ; FIGNL1
1 1.000 0.120 7 50497706 intron variant T/C snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs10821938
rs10821938
ARID5B
2 0.925 0.120 10 61965014 intron variant A/C snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs10899736
rs10899736
DDC ; FIGNL1
1 1.000 0.120 7 50479227 intron variant G/A;C snv 0.700 1.000 1 2013 2013