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: rs11088309
rs11088309
RUNX1
2 0.925 0.080 21 35092334 intron variant C/A;G snv 9.3E-02 0.700 1.000 2 2019 2019
dbSNP: rs1775554
rs1775554 		3 0.882 0.080 10 9012377 intergenic variant A/C snv 0.35 0.700 1.000 2 2019 2019
dbSNP: rs1837253
rs1837253 		10 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 0.700 1.000 2 2019 2019
dbSNP: rs34290285
rs34290285
D2HGDH
8 0.851 0.120 2 241759225 intron variant G/A snv 0.27 0.700 1.000 2 2019 2019
dbSNP: rs7936312
rs7936312 		5 0.882 0.080 11 76582682 intergenic variant G/T snv 0.44 0.700 1.000 2 2019 2019
dbSNP: rs992969
rs992969 		4 0.882 0.080 9 6209697 intergenic variant A/G;T snv 0.700 1.000 2 2019 2019
dbSNP: rs10414065
rs10414065 		4 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs1059513
rs1059513
NAB2 ; STAT6
11 0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs10667251
rs10667251 		4 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 0.700 1.000 1 2019 2019
dbSNP: rs10699671
rs10699671
NDFIP1
2 0.925 0.080 5 142139375 intron variant -/AGG delins 0.68 0.700 1.000 1 2019 2019
dbSNP: rs10795672
rs10795672 		2 0.925 0.080 10 8735677 intergenic variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1117490
rs1117490
TRIM26
2 0.925 0.080 6 30202733 intron variant T/C snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs11178648
rs11178648
TSPAN8
2 0.925 0.080 12 71139430 intron variant C/T snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs11255504
rs11255504
GATA3
2 0.925 0.080 10 8062378 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11715524
rs11715524
TFRC
3 0.925 0.080 3 196035621 intron variant G/A snv 0.54 0.700 1.000 1 2019 2019
dbSNP: rs11742240
rs11742240 		2 0.925 0.080 5 35881274 downstream gene variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs117710327
rs117710327 		5 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs12470864
rs12470864
IL1RL1
4 0.925 0.080 2 102309902 upstream gene variant G/A snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs12617922
rs12617922 		1 1.000 2 145399111 intergenic variant G/A snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs12722502
rs12722502
IL2RA
4 0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03 0.700 1.000 1 2019 2019
dbSNP: rs12788104
rs12788104 		1 1.000 11 1129831 regulatory region variant A/G snv 0.55 0.700 1.000 1 2019 2019
dbSNP: rs1321859
rs1321859
LOC105377891
2 0.925 0.080 6 90301954 intron variant C/T snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs174535
rs174535
MYRF ; TMEM258
19 0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 0.700 1.000 1 2019 2019
dbSNP: rs17454584
rs17454584 		6 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs174621
rs174621
FADS2
2 1.000 11 61862632 non coding transcript exon variant G/A;C snv 0.700 1.000 1 2019 2019