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: rs116908763
rs116908763
CTDSPL2
1 15 44427813 5 prime UTR variant C/T snv 2.3E-02 0.700 1.000 2 2016 2019
dbSNP: rs117565673
rs117565673
CBFA2T3
1 16 88977046 5 prime UTR variant T/C snv 3.7E-02 0.700 1.000 2 2016 2019
dbSNP: rs144991697
rs144991697
MIDEAS
1 14 73771327 intron variant G/A snv 1.6E-02 0.700 1.000 2 2016 2019
dbSNP: rs58123204
rs58123204 		1 12 53366378 intergenic variant A/C;G snv 0.700 1.000 2 2016 2019
dbSNP: rs77697190
rs77697190 		1 14 103380462 upstream gene variant C/T snv 7.9E-02 0.700 1.000 2 2016 2019
dbSNP: rs1004531
rs1004531
TNFAIP8
1 5 119269328 intron variant C/T snv 0.56 0.700 1.000 1 2019 2019
dbSNP: rs10123382
rs10123382 		1 9 4757649 intron variant G/A snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs10128757
rs10128757
TBK1
1 12 64467594 intron variant T/C snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs10148930
rs10148930
EVL
1 14 100134466 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10182296
rs10182296
NEB ; RIF1
1 2 151515219 intron variant G/A snv 0.61 0.700 1.000 1 2019 2019
dbSNP: rs10210063
rs10210063
ZEB2
1 2 144425390 intron variant C/G snv 7.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs10277403
rs10277403 		1 7 47594213 intergenic variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs10402931
rs10402931
PDCD5
1 19 32581163 upstream gene variant G/A;C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1041070
rs1041070
SUCLA2 ; LINC00562 ; LINC00444
1 13 47931358 non coding transcript exon variant C/T snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs10411508
rs10411508
KCNN1 ; ARRDC2
1 19 17999765 3 prime UTR variant G/A snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs1043407
rs1043407
RAB8A ; HSH2D
1 19 16133416 3 prime UTR variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1044778
rs1044778
CHD2
1 15 93027556 3 prime UTR variant G/C snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs10457234
rs10457234
SLC16A10
1 6 111137788 intron variant T/C snv 0.72 0.700 1.000 1 2019 2019
dbSNP: rs1045911
rs1045911
TMEM14C
1 6 10723216 5 prime UTR variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10463065
rs10463065 		1 5 177322927 intergenic variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs1046411
rs1046411
CNNM2
1 10 103078059 3 prime UTR variant G/A snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs1048310
rs1048310
ATF4 ; MIEF1
1 22 39517277 3 prime UTR variant T/G snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs1049212
rs1049212
PPL
1 16 4882928 3 prime UTR variant A/G snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs10495161
rs10495161 		1 1 220963330 regulatory region variant C/T snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs10496344
rs10496344
AFF3
1 2 100147663 intron variant T/C;G snv 0.700 1.000 1 2019 2019