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: rs7158663
rs7158663
MEG3
9 0.827 0.240 14 100853087 non coding transcript exon variant A/G snv 0.42 0.010 < 0.001 1 2016 2016
dbSNP: rs2186607
rs2186607
TRPC6
10 0.776 0.080 11 101785666 intron variant T/A snv 0.51 0.700 1.000 1 2019 2019
dbSNP: rs1414521156
rs1414521156
SLCO6A1
1 5 102459731 missense variant T/A;C snv 4.0E-06; 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs4450168
rs4450168
SBF2
9 0.790 0.080 11 10265208 intron variant A/C;T snv 0.12 0.700 1.000 1 2019 2019
dbSNP: rs4919687
rs4919687
CYP17A1
14 0.742 0.160 10 102835491 non coding transcript exon variant G/A snv 0.25 0.700 1.000 1 2016 2016
dbSNP: rs12548629
rs12548629
BAALC ; BAALC-AS1
10 0.776 0.120 8 103189173 intron variant C/T snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs141752671
rs141752671 		17 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 0.700 1.000 1 2016 2016
dbSNP: rs148883465
rs148883465 		17 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 0.700 1.000 1 2016 2016
dbSNP: rs17035289
rs17035289 		9 0.790 0.080 4 105127134 intergenic variant T/C snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs7679673
rs7679673 		28 0.677 0.440 4 105140377 intron variant C/A snv 0.50 0.700 1.000 1 2016 2016
dbSNP: rs17035310
rs17035310 		10 0.790 0.080 4 105143597 upstream gene variant C/T snv 0.14 0.700 1.000 1 2015 2015
dbSNP: rs1391441
rs1391441
TET2 ; TET2-AS1
11 0.763 0.240 4 105207603 intron variant G/A snv 0.70 0.700 1.000 1 2019 2019
dbSNP: rs6928864
rs6928864 		9 0.790 0.080 6 105519019 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1512436
rs1512436 		10 0.790 0.080 11 106436144 intergenic variant T/C snv 0.50 0.700 1.000 1 2015 2015
dbSNP: rs1078643
rs1078643
TMEM238L ; TMEM220-AS1
10 0.776 0.080 17 10803924 missense variant G/A;C snv 0.700 1.000 3 2019 2019
dbSNP: rs9583269
rs9583269
MYO16
9 0.790 0.080 13 108630682 intron variant C/T snv 0.34 0.700 1.000 1 2017 2017
dbSNP: rs770292690
rs770292690
TCHP
1 12 109908872 missense variant C/T snv 5.6E-05 9.8E-05 0.010 1.000 1 2016 2016
dbSNP: rs7993934
rs7993934
COL4A2
9 0.790 0.080 13 110422568 intron variant C/T snv 0.56 0.700 1.000 1 2019 2019
dbSNP: rs8000189
rs8000189
COL4A2
10 0.776 0.080 13 110423534 intron variant C/T snv 0.61 0.700 1.000 1 2019 2019
dbSNP: rs9481067
rs9481067
SLC22A16
10 0.776 0.080 6 110429349 intron variant A/G snv 0.58 0.700 1.000 1 2018 2018
dbSNP: rs10980628
rs10980628
LPAR1
10 0.776 0.080 9 110909123 intron variant T/C snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs4849303
rs4849303
ACOXL
9 0.790 0.080 2 110970905 intron variant C/G;T snv 0.700 1.000 1 2014 2014
dbSNP: rs587777894
rs587777894
MTOR
9 0.776 0.240 1 11124516 missense variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519917
rs1057519917
MTOR
7 0.807 0.160 1 11124517 missense variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs3087967
rs3087967
C11orf53
10 0.776 0.080 11 111286111 3 prime UTR variant T/C snv 0.72 0.700 1.000 2 2019 2019