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: rs10085617
rs10085617
SDK1
1 1.000 7 3595079 intron variant A/T snv 0.66 0.700 1.000 1 2018 2018
dbSNP: rs10499
rs10499
ATP2A1 ; RABEP2
1 1.000 16 28904206 3 prime UTR variant G/A;T snv 0.70 0.700 1.000 1 2018 2018
dbSNP: rs11210887
rs11210887
PTPRF
2 0.925 0.040 1 43610348 intron variant G/A snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs113551349
rs113551349
SLC6A9
2 0.925 0.040 1 44009451 intron variant C/T snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs12003072
rs12003072 		1 1.000 9 84156246 intergenic variant C/A snv 3.2E-02 0.700 1.000 1 2015 2015
dbSNP: rs139868495
rs139868495
LINC01288
2 0.925 0.040 8 34805452 intron variant C/T snv 3.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs142324060
rs142324060
LOC101929710 ; MIR583HG
1 1.000 5 96090053 intron variant A/G snv 7.2E-03 0.700 1.000 1 2015 2015
dbSNP: rs142981069
rs142981069 		1 1.000 18 61158789 intergenic variant A/G snv 9.1E-03 0.700 1.000 1 2015 2015
dbSNP: rs1448602
rs1448602
CADM2
1 1.000 3 85731304 intron variant A/G;T snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs145108385
rs145108385
LOC648987
2 0.925 0.040 5 43054645 intron variant A/G snv 0.700 1.000 1 2019 2019
dbSNP: rs1476535
rs1476535
FOXP2
2 0.925 0.040 7 114430980 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1574587
rs1574587
ATP2C2
1 1.000 16 84419450 intron variant C/T snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs17761723
rs17761723
SMG6
1 1.000 17 2203796 intron variant C/T snv 0.25 0.700 1.000 1 2018 2018
dbSNP: rs2099149
rs2099149 		1 1.000 12 30326425 downstream gene variant T/G snv 0.28 0.700 1.000 1 2016 2016
dbSNP: rs2189012
rs2189012
FOXP2
2 0.925 0.040 7 114571857 intron variant G/A snv 0.73 0.700 1.000 1 2019 2019
dbSNP: rs2391769
rs2391769
LOC105378866
3 0.925 0.040 1 96513405 regulatory region variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2782639
rs2782639
PTPRF
2 0.925 0.040 1 43540668 intron variant A/G snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs2875907
rs2875907
CADM2
2 0.925 0.040 3 85469430 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs4259397
rs4259397 		2 0.925 0.040 8 92354062 upstream gene variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs4471463
rs4471463
NCAM1
1 1.000 11 113112873 intron variant C/T snv 0.57 0.700 1.000 1 2016 2016
dbSNP: rs4858253
rs4858253 		2 0.925 0.040 3 20687599 intron variant C/T snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs4916723
rs4916723
LINC00461
4 0.925 0.040 5 88558577 intron variant A/C;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs56319043
rs56319043
ST3GAL3 ; KDM4A ; KDM4A-AS1
2 0.925 0.040 1 43705540 intron variant C/T snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs74760947
rs74760947 		2 0.925 0.040 8 34495092 intergenic variant A/G snv 3.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs7651996
rs7651996
CADM2
1 1.000 3 85008198 intron variant G/A;T snv 0.700 1.000 1 2018 2018