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: rs1548514
rs1548514 		1 1.000 0.040 6 30419691 downstream gene variant G/A;C;T snv 0.700 1.000 1 2010 2010
dbSNP: rs16843742
rs16843742
PTPRC
1 1.000 0.040 1 198703170 intron variant T/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs17188127
rs17188127
TRIM15
1 1.000 0.040 6 30167325 intron variant C/T snv 9.9E-03 0.700 1.000 1 2010 2010
dbSNP: rs17188268
rs17188268 		1 1.000 0.040 6 30231581 downstream gene variant G/A snv 3.2E-02 0.700 1.000 1 2010 2010
dbSNP: rs17190134
rs17190134
HCG22
1 1.000 0.040 6 31054083 non coding transcript exon variant C/A;G snv 0.700 1.000 1 2010 2010
dbSNP: rs17195551
rs17195551
ATAT1
1 1.000 0.040 6 30633618 intron variant C/T snv 3.2E-02 0.700 1.000 1 2010 2010
dbSNP: rs199559999
rs199559999
STAT4
1 1.000 0.040 2 191090480 intron variant TAC/- del 0.700 1.000 1 2016 2016
dbSNP: rs2017445
rs2017445
IKZF4 ; LOC105369781
1 1.000 0.040 12 56013288 intron variant G/A;C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs2236313
rs2236313
RNASET2
1 1.000 0.040 6 166946901 intron variant T/C snv 0.53 0.50 0.800 1.000 1 2010 2010
dbSNP: rs2247314
rs2247314
RNASET2
1 1.000 0.040 6 166956742 intron variant T/C snv 0.42 0.700 1.000 1 2016 2016
dbSNP: rs2248902
rs2248902 		1 1.000 0.040 6 31266337 downstream gene variant G/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs2523505
rs2523505
DDX39B ; SNORD84 ; ATP6V1G2-DDX39B ; DDX39B-AS1
1 1.000 0.040 6 31542225 5 prime UTR variant C/G snv 7.6E-02 0.700 1.000 1 2010 2010
dbSNP: rs2687812
rs2687812
TG
1 1.000 0.040 8 132918810 intron variant A/T snv 0.41 0.700 1.000 1 2016 2016
dbSNP: rs28383344
rs28383344
HLA-DQA1 ; LOC107986589
1 1.000 0.040 6 32637290 intron variant C/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs2839511
rs2839511
UBASH3A
1 1.000 0.040 21 42428412 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs3130347
rs3130347
PPT2 ; EGFL8 ; PPT2-EGFL8
1 1.000 0.040 6 32166879 intron variant T/C snv 0.15 0.18 0.700 1.000 1 2010 2010
dbSNP: rs3130455
rs3130455
TCF19 ; CCHCR1
1 1.000 0.040 6 31158201 5 prime UTR variant A/C;T snv 0.700 1.000 1 2010 2010
dbSNP: rs3132649
rs3132649 		1 1.000 0.040 6 30353280 downstream gene variant G/A snv 0.11 0.700 1.000 1 2010 2010
dbSNP: rs3218822
rs3218822
GTF2H4 ; VARS2
1 1.000 0.040 6 30912559 intron variant T/C snv 1.9E-02 0.700 1.000 1 2010 2010
dbSNP: rs33986393
rs33986393 		1 1.000 0.040 6 30456297 downstream gene variant A/G snv 0.16 0.700 1.000 1 2010 2010
dbSNP: rs34101875
rs34101875 		1 1.000 0.040 6 30455581 non coding transcript exon variant G/A;C;T snv 0.700 1.000 1 2010 2010
dbSNP: rs34346645
rs34346645
FOXP1
1 1.000 0.040 3 71508794 intron variant C/A snv 0.32 0.700 1.000 1 2016 2016
dbSNP: rs35161626
rs35161626
UBE2E2
1 1.000 0.040 3 23470822 intron variant A/- del 0.64 0.700 1.000 1 2016 2016
dbSNP: rs35407515
rs35407515 		1 1.000 0.040 6 30455446 non coding transcript exon variant A/G snv 0.17 0.700 1.000 1 2010 2010
dbSNP: rs35792611
rs35792611
LOC105375012
1 1.000 0.040 6 30463098 upstream gene variant C/G snv 0.16 0.700 1.000 1 2010 2010