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: rs2524079
rs2524079
HLA-B
6 6 31274397 intron variant G/A snv 0.44 0.700 1.000 2 2011 2017
dbSNP: rs1001745
rs1001745
RHOQ
1 2 46547920 intron variant T/C snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs10022109
rs10022109
TET2
1 4 105166665 intron variant A/G snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs10076188
rs10076188
MCTP1 ; SLF1
1 5 94726834 intron variant C/T snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs10087240
rs10087240
PVT1
2 8 128000328 intron variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1014530
rs1014530
TRAF1
1 9 120922814 intron variant T/C snv 0.51 0.700 1.000 1 2016 2016
dbSNP: rs10401193
rs10401193
GATAD2A
2 19 19480257 intron variant A/G snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs10404046
rs10404046
EPS15L1
1 19 16366444 intron variant G/C snv 0.63 0.700 1.000 1 2018 2018
dbSNP: rs10408945
rs10408945
EPS15L1
1 19 16466180 intron variant G/T snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs10411936
rs10411936
EPS15L1
3 1.000 0.080 19 16437564 intron variant A/G snv 0.63 0.700 1.000 1 2011 2011
dbSNP: rs10424282
rs10424282
VRK3
1 19 49989603 intron variant C/G;T snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs10489208
rs10489208
GPR161
1 1 168125471 intron variant C/T snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs10496125
rs10496125
SPRED2
1 2 65408072 intron variant C/A snv 9.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs10554441
rs10554441
ETV1
1 7 13978399 intron variant ACACACAC/-;AC;ACAC;ACACAC;ACACACACAC;ACACACACACAC delins 0.78 0.700 1.000 1 2016 2016
dbSNP: rs10554589
rs10554589
ANKRD11 ; LOC105371414
1 16 89295870 intron variant ATGTG/- delins 0.83 0.700 1.000 1 2016 2016
dbSNP: rs10768983
rs10768983
HSD17B12
1 11 43818385 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs10777181
rs10777181
POC1B
1 12 89514850 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs10805888
rs10805888
LINC01331
1 5 74489722 intron variant A/G snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs10828723
rs10828723
PRTFDC1
1 10 24916129 intron variant T/C snv 0.26 0.700 1.000 1 2016 2016
dbSNP: rs10844706
rs10844706
CD69
1 12 9757536 intron variant C/A snv 0.34 0.700 1.000 1 2016 2016
dbSNP: rs10867411
rs10867411
TLE4
1 9 79683075 intron variant A/G snv 0.52 0.700 1.000 1 2016 2016
dbSNP: rs10886369
rs10886369 		1 10 119024129 intron variant A/G snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs10901450
rs10901450
UROS
1 10 125820725 intron variant G/C snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs11024625
rs11024625
GTF2H1 ; LOC105376577
1 11 18350013 intron variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs11064237
rs11064237
NCAPD2
1 12 6504990 intron variant T/C snv 0.34 0.700 1.000 1 2012 2012