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: rs11866328
rs11866328
GRIN2A
3 0.925 0.120 16 9768699 intron variant G/T snv 0.38 0.810 1.000 1 2011 2011
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 2011 2011
dbSNP: rs12649554
rs12649554 		1 1.000 0.080 4 100975519 regulatory region variant T/C snv 0.65 0.700 1.000 1 2011 2011
dbSNP: rs12663103
rs12663103
GPSM3
7 0.851 0.240 6 32193547 intron variant T/C snv 6.1E-02 0.700 1.000 1 2011 2011
dbSNP: rs13199787
rs13199787 		2 0.925 0.200 6 32737499 upstream gene variant C/T snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs1383265
rs1383265 		2 0.925 0.200 6 32772111 intergenic variant T/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs154972
rs154972 		2 0.925 0.120 6 32932874 downstream gene variant A/G snv 0.35 0.700 1.000 1 2011 2011
dbSNP: rs16855458
rs16855458
XRCC5
2 0.925 0.120 2 216146098 intron variant C/A snv 0.16 0.010 1.000 1 2011 2011
dbSNP: rs204999
rs204999 		13 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs2301226
rs2301226
HLA-DPA1
1 1.000 0.080 6 33066819 non coding transcript exon variant G/A snv 0.16 0.700 1.000 1 2011 2011
dbSNP: rs2301271
rs2301271
HLA-DQB2
3 0.882 0.240 6 32757416 intron variant A/G snv 0.60 0.700 1.000 1 2011 2011
dbSNP: rs2395174
rs2395174 		5 0.827 0.320 6 32437101 upstream gene variant T/G snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs2836389
rs2836389
ERG
1 1.000 0.080 21 38431740 intron variant T/C snv 0.27 0.700 1.000 1 2011 2011
dbSNP: rs2854028
rs2854028
RING1
1 1.000 0.080 6 33211912 missense variant C/A;T snv 2.7E-05; 0.22 0.700 1.000 1 2011 2011
dbSNP: rs2896019
rs2896019
PNPLA3
10 0.790 0.160 22 43937814 intron variant T/G snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs3104404
rs3104404 		2 0.925 0.160 6 32714397 upstream gene variant C/A snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs3117039
rs3117039
HLA-DPB2
2 0.925 0.160 6 33118074 intron variant C/T snv 0.35 0.700 1.000 1 2011 2011
dbSNP: rs3130215
rs3130215
COL11A2P1
3 0.882 0.240 6 33107186 intron variant A/G snv 0.69 0.700 1.000 1 2011 2011
dbSNP: rs3782886
rs3782886
BRAP
22 0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 0.700 1.000 1 2011 2011
dbSNP: rs385893
rs385893 		9 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 0.700 1.000 1 2011 2011
dbSNP: rs421446
rs421446
RING1 ; HSD17B8 ; MIR219A1
3 0.882 0.280 6 33207006 upstream gene variant A/G snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs423639
rs423639 		3 0.882 0.240 6 33019997 intergenic variant C/T snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs430397
rs430397
HSPA5
9 0.763 0.240 9 125238840 intron variant C/T snv 9.1E-02 0.11 0.010 1.000 1 2011 2011
dbSNP: rs439205
rs439205
HSD17B8 ; MIR219A1
2 0.925 0.200 6 33206065 intron variant G/A snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs4711332
rs4711332
ITPR3
2 0.925 0.200 6 33627622 intron variant A/G snv 0.86 0.700 1.000 1 2011 2011