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: rs11622435
rs11622435
LOC101928462
7 0.827 0.120 14 81151652 intron variant G/A snv 4.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs11645800
rs11645800 		1 1.000 0.080 16 62966386 intergenic variant A/G snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs116510623
rs116510623 		1 1.000 0.080 11 24209937 intergenic variant A/G snv 2.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs11662622
rs11662622 		2 1.000 0.080 18 65592400 intergenic variant A/G snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs1171614
rs1171614
SLC16A9
7 0.882 0.200 10 59709780 5 prime UTR variant T/C snv 0.79 0.700 1.000 1 2018 2018
dbSNP: rs1171616
rs1171616
SLC16A9
6 0.882 0.200 10 59708831 intron variant G/T snv 0.79 0.700 1.000 1 2018 2018
dbSNP: rs117329947
rs117329947
C12orf75 ; LOC105369957
1 1.000 0.080 12 105391125 intron variant A/C snv 2.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs117897666
rs117897666
LOC105370892
3 0.882 0.160 15 73811619 intergenic variant C/T snv 0.700 1.000 1 2018 2018
dbSNP: rs117935223
rs117935223
PRODH
2 1.000 0.080 22 18923820 non coding transcript exon variant C/A snv 0.700 1.000 1 2018 2018
dbSNP: rs11959928
rs11959928
C9 ; DAB2
4 1.000 0.080 5 39397030 intron variant T/A snv 0.39 0.700 1.000 1 2010 2010
dbSNP: rs12032578
rs12032578
LINC00624
1 1.000 0.080 1 147339048 intron variant T/C snv 4.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs12134854
rs12134854
SLC44A5
2 1.000 0.080 1 75671921 intron variant T/C snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs12194000
rs12194000
SLC22A16
2 1.000 0.080 6 110454809 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs12207180
rs12207180
SLC22A2
2 1.000 0.080 6 160212075 intron variant T/A;G snv 0.12 0.700 1.000 1 2019 2019
dbSNP: rs1242780
rs1242780
PTPRN2
2 1.000 0.080 7 157757146 intron variant T/G snv 0.25 0.700 1.000 1 2018 2018
dbSNP: rs12509595
rs12509595 		10 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs1260326
rs1260326
GCKR
81 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 1 2010 2010
dbSNP: rs12634709
rs12634709
LOC105377110
2 1.000 0.080 3 59603270 intron variant G/T snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs12963285
rs12963285 		1 1.000 0.080 18 57097183 intergenic variant T/C snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs13084795
rs13084795 		1 1.000 0.080 3 152612677 intergenic variant G/A snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs13111638
rs13111638
SLC2A9 ; LOC105374476
4 0.882 0.200 4 9995266 intron variant T/C snv 0.82 0.700 1.000 1 2018 2018
dbSNP: rs1317947
rs1317947
MMP20 ; LOC101928477
2 1.000 0.080 11 102617342 intron variant G/A snv 0.41 0.700 1.000 1 2018 2018
dbSNP: rs13230625
rs13230625 		3 1.000 0.080 7 1246608 regulatory region variant G/A snv 0.62 0.700 1.000 1 2019 2019
dbSNP: rs13329952
rs13329952
UMOD
3 1.000 0.080 16 20355185 intron variant T/C snv 0.24 0.700 1.000 1 2016 2016
dbSNP: rs13538
rs13538
NAT8 ; ALMS1P1
5 1.000 0.080 2 73641201 missense variant A/G snv 0.21 0.31 0.700 1.000 1 2010 2010