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: rs2297497
rs2297497
ABHD12
1 20 25317273 intron variant G/A snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs2427590
rs2427590
PRPF6
1 20 64010704 intron variant T/C snv 0.26 0.700 1.000 1 2012 2012
dbSNP: rs259981
rs259981
ZNF831
1 20 59173314 intron variant T/A snv 0.50 0.700 1.000 1 2016 2016
dbSNP: rs3746410
rs3746410
FER1L4
1 20 35602948 intron variant A/G snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs4602269
rs4602269
PTPN1
1 20 50555698 intron variant C/T snv 5.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs4618126
rs4618126
PDYN-AS1
1 20 1950239 intron variant G/A snv 0.43 0.700 1.000 1 2016 2016
dbSNP: rs4911253
rs4911253
DNMT3B
1 20 32764779 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs6051761
rs6051761
C20orf194
1 20 3340921 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs6122940
rs6122940 		1 20 50489248 intergenic variant G/T snv 0.12 0.700 1.000 1 2016 2016
dbSNP: rs804382
rs804382 		1 20 21449210 intergenic variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs10401193
rs10401193
GATAD2A
2 19 19480257 intron variant A/G snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs10404046
rs10404046
EPS15L1
1 19 16366444 intron variant G/C snv 0.63 0.700 1.000 1 2018 2018
dbSNP: rs10408945
rs10408945
EPS15L1
1 19 16466180 intron variant G/T snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs10411936
rs10411936
EPS15L1
3 1.000 0.080 19 16437564 intron variant A/G snv 0.63 0.700 1.000 1 2011 2011
dbSNP: rs10422126
rs10422126
LOC284454 ; MIR23A ; MIR24-2 ; MIR27A
2 19 13837498 non coding transcript exon variant G/A snv 0.37 0.700 1.000 1 2016 2016
dbSNP: rs10424282
rs10424282
VRK3
1 19 49989603 intron variant C/G;T snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs10425451
rs10425451 		1 19 54441331 upstream gene variant C/T snv 0.39 0.700 1.000 1 2012 2012
dbSNP: rs1062808
rs1062808
CARD8
1 19 48208219 3 prime UTR variant T/C snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs11669741
rs11669741 		1 19 58449114 upstream gene variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs12459634
rs12459634
KMT2B ; IGFLR1
2 19 35739273 3 prime UTR variant T/C snv 0.13 0.11 0.700 1.000 1 2012 2012
dbSNP: rs12459781
rs12459781
APBA3 ; MRPL54 ; LOC105372248
1 19 3762121 upstream gene variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs12981683
rs12981683
ARRDC2
1 19 18003191 intron variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs12981732
rs12981732
LOC107985325
1 19 55013007 intron variant C/G;T snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs13535
rs13535
ZNF559 ; ZNF559-ZNF177
1 19 9343497 3 prime UTR variant A/G snv 0.61 0.700 1.000 1 2012 2012
dbSNP: rs2305806
rs2305806
SH2D3A
2 1.000 0.120 19 6754996 synonymous variant T/C snv 0.30 0.35 0.700 1.000 1 2012 2012