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: rs117222687
rs117222687
ARVCF ; COMT
2 22 19968491 intron variant G/C snv 3.8E-02 4.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs4820323
rs4820323
PLA2G6 ; MAFF
4 22 38203760 non coding transcript exon variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs7445
rs7445
UBE2L3
2 22 21622758 3 prime UTR variant C/G;T snv 0.22 0.700 1.000 1 2019 2019
dbSNP: rs235314
rs235314
PTTG1IP
3 21 44851537 missense variant C/T snv 0.48 0.46 0.700 1.000 1 2019 2019
dbSNP: rs2410182
rs2410182 		2 21 39808149 intergenic variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs2837253
rs2837253 		2 21 39849329 intergenic variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1800961
rs1800961
HNF4A
21 0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs2050058
rs2050058
ZHX3
2 20 41278348 intron variant G/A snv 0.48 0.700 1.000 1 2019 2019
dbSNP: rs2328223
rs2328223 		3 20 17865277 intergenic variant A/C;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs259983
rs259983
ZNF831
2 20 59160402 5 prime UTR variant A/C snv 0.25 0.700 1.000 1 2018 2018
dbSNP: rs4260308
rs4260308 		2 20 10981537 intron variant G/A snv 0.41 0.700 1.000 1 2018 2018
dbSNP: rs459588
rs459588
ZNF831
2 20 59139712 intron variant A/C snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs4911477
rs4911477
PROCR ; MMP24-AS1-EDEM2
2 20 35193182 intron variant T/C snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs6026740
rs6026740
ZNF831
3 20 59165293 intron variant A/G snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs6063050
rs6063050
EYA2
2 20 46975601 intron variant T/C snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs6073958
rs6073958 		4 20 45923216 downstream gene variant T/C snv 0.22 0.700 1.000 1 2019 2019
dbSNP: rs6081377
rs6081377
LINC00652 ; LINC00653
1 20 18796142 upstream gene variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs6108787
rs6108787 		5 20 10986566 intron variant T/G snv 0.46 0.700 1.000 1 2018 2018
dbSNP: rs73306896
rs73306896
ZNF831
2 20 59175478 intron variant C/T snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs79263055
rs79263055
ZNF831
2 20 59175423 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs116843064
rs116843064
ANGPTL4
16 0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs12978472
rs12978472
INSR
5 19 7257979 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs142673685
rs142673685 		1 19 31669942 intergenic variant C/T snv 4.0E-03 0.700 1.000 1 2018 2018
dbSNP: rs143020224
rs143020224
SMARCA4
2 19 11076648 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1531517
rs1531517 		7 1.000 0.080 19 44738916 intergenic variant G/A snv 0.11 0.700 1.000 1 2019 2019