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: rs1800872
rs1800872
IL10 ; IL19
119 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.700 0
dbSNP: rs10501678
rs10501678
GRM5
4 1.000 11 88708934 intron variant C/T snv 3.1E-02 0.700 1.000 1 2009 2009
dbSNP: rs1051794
rs1051794
MICA
5 0.925 0.120 6 31411332 missense variant G/A snv 0.34 0.35 0.700 1.000 1 2009 2009
dbSNP: rs1062470
rs1062470
CDSN ; PSORS1C1
5 0.925 0.040 6 31116658 synonymous variant G/A snv 0.37 0.41 0.700 1.000 1 2009 2009
dbSNP: rs12122100
rs12122100
NBPF13P ; LOC728989
4 1.000 1 147037378 intron variant T/C snv 0.76 0.800 1.000 1 2009 2009
dbSNP: rs12185555
rs12185555 		4 1.000 2 226694601 regulatory region variant A/G snv 0.25 0.700 1.000 1 2009 2009
dbSNP: rs12274302
rs12274302
DISC1FP1
4 1.000 11 90853732 non coding transcript exon variant C/A;G;T snv 0.800 1.000 1 2009 2009
dbSNP: rs12697941
rs12697941
MUCL3 ; SFTA2
4 1.000 6 30936937 intron variant G/A snv 0.18 0.700 1.000 1 2009 2009
dbSNP: rs13191519
rs13191519
HLA-B ; LINC02571 ; LOC112267902
4 1.000 6 31297975 intron variant T/C snv 0.12 0.700 1.000 1 2009 2009
dbSNP: rs13207315
rs13207315
HLA-B ; HLA-C
4 1.000 6 31273350 intron variant T/C snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs13216197
rs13216197
HLA-B ; LINC02571 ; LOC112267902
4 1.000 6 31303241 intron variant T/C snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs13394720
rs13394720 		6 1.000 2 233593475 intergenic variant T/C snv 7.0E-02 0.800 1.000 1 2009 2009
dbSNP: rs16914280
rs16914280
GRM5
4 1.000 11 88588556 intron variant C/T snv 4.7E-02 0.800 1.000 1 2009 2009
dbSNP: rs16948255
rs16948255 		4 1.000 16 74847922 downstream gene variant C/T snv 3.9E-02 0.800 1.000 1 2009 2009
dbSNP: rs17291045
rs17291045
LINC02477
4 1.000 4 160585745 intron variant C/T snv 9.3E-02 0.800 1.000 1 2009 2009
dbSNP: rs17324272
rs17324272 		4 1.000 X 133003128 intergenic variant T/C snv 3.2E-03 0.800 1.000 1 2009 2009
dbSNP: rs1777672
rs1777672
NBEA
4 1.000 13 35603682 intron variant G/A snv 0.94 0.800 1.000 1 2009 2009
dbSNP: rs1894406
rs1894406
HLA-DOB
5 0.925 0.120 6 32819279 intron variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs2071472
rs2071472
HLA-DOB
5 0.925 0.120 6 32816843 intron variant C/T snv 0.34 0.27 0.700 1.000 1 2009 2009
dbSNP: rs2071473
rs2071473
HLA-DOB
4 1.000 6 32814828 intron variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs2071474
rs2071474
HLA-DOB
5 0.925 0.120 6 32814805 intron variant C/T snv 0.27 0.700 1.000 1 2009 2009
dbSNP: rs2074479
rs2074479
RNF39
4 1.000 6 30073232 missense variant A/G snv 0.15 0.17 0.700 1.000 1 2009 2009
dbSNP: rs2074480
rs2074480
RNF39
4 1.000 6 30073033 intron variant T/G snv 0.17 0.700 1.000 1 2009 2009
dbSNP: rs2156875
rs2156875
HLA-B
6 0.882 0.200 6 31349570 intron variant C/T snv 0.50 0.700 1.000 1 2009 2009
dbSNP: rs2219893
rs2219893 		5 0.925 0.120 6 32801886 intergenic variant T/C snv 0.33 0.700 1.000 1 2009 2009