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: rs1371799
rs1371799 		1 4 74112120 upstream gene variant T/C snv 0.49 0.800 1.000 1 2011 2011
dbSNP: rs16993221
rs16993221
RUNX1 ; LOC100506403
1 21 35477121 intron variant A/T snv 2.6E-02 0.800 1.000 1 2013 2013
dbSNP: rs17609240
rs17609240
GSDMA
1 17 39954436 intron variant T/A;G snv 0.800 1.000 1 2009 2009
dbSNP: rs2227139
rs2227139 		4 0.925 0.160 6 32445682 downstream gene variant G/A snv 0.61 0.800 1.000 1 2009 2009
dbSNP: rs2517510
rs2517510 		1 6 31062345 downstream gene variant T/G snv 0.45 0.800 1.000 1 2011 2011
dbSNP: rs7600502
rs7600502 		1 2 22074131 intron variant A/G snv 1.4E-02 0.800 1.000 1 2013 2013
dbSNP: rs10016631
rs10016631
POLR2B
1 4 57019797 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1006310
rs1006310
ATF6
1 1 161841765 intron variant T/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs10075801
rs10075801
SLC22A4 ; MIR3936HG
5 5 132341949 intron variant A/G snv 0.31 0.700 1.000 1 2016 2016
dbSNP: rs10087240
rs10087240
PVT1
2 8 128000328 intron variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10094382
rs10094382
CHD7
1 8 60860726 intron variant C/T snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs10098310
rs10098310
CCDC26
3 8 129601368 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1010109
rs1010109
ARHGAP26
1 5 143174597 intron variant A/G snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs10120452
rs10120452
GABBR2
1 9 98623959 intron variant G/A snv 0.17 0.700 1.000 1 2011 2011
dbSNP: rs10129035
rs10129035 		1 12 83706429 intergenic variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs10138752
rs10138752
RAD51B
5 14 68713254 intron variant C/T snv 8.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs10146637
rs10146637
FBXO34
2 14 55278092 intron variant G/A snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs1015022
rs1015022
ERG ; LOC105372802
1 21 38507058 intron variant G/C snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs10158210
rs10158210 		1 1 158342195 intergenic variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1016680
rs1016680 		1 17 37514283 downstream gene variant A/C snv 0.74 0.700 1.000 1 2019 2019
dbSNP: rs10178094
rs10178094
RBMS1
1 2 160479895 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10178249
rs10178249
CNTNAP5
1 2 124696819 intron variant A/G snv 0.42 0.700 1.000 1 2011 2011
dbSNP: rs10206089
rs10206089 		4 2 61476184 intron variant G/A snv 0.700 1.000 1 2016 2016
dbSNP: rs10215854
rs10215854
CPSF4 ; PTCD1 ; ATP5MF-PTCD1
2 7 99439297 intron variant G/A snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs1023667
rs1023667 		1 5 158541893 intron variant G/A;C snv 0.700 1.000 1 2019 2019