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: rs1356122
rs1356122 		1 1.000 0.080 3 154465773 intergenic variant G/A;C snv 0.700 1.000 1 2007 2007
dbSNP: rs1438131
rs1438131 		1 1.000 0.080 2 23283911 regulatory region variant G/A snv 0.34 0.700 1.000 1 2007 2007
dbSNP: rs1449263
rs1449263 		5 1.000 0.080 2 181454574 upstream gene variant C/T snv 0.56 0.010 1.000 1 2007 2007
dbSNP: rs151719
rs151719
HLA-DMB
2 0.925 0.160 6 32936123 non coding transcript exon variant C/T snv 0.72 0.700 1.000 1 2007 2007
dbSNP: rs1610603
rs1610603
HLA-F ; HLA-F-AS1
1 1.000 0.080 6 29740445 intron variant T/A;C snv 0.700 1.000 1 2007 2007
dbSNP: rs1610630
rs1610630 		1 1.000 0.080 6 29761509 intron variant C/T snv 0.81 0.700 1.000 1 2007 2007
dbSNP: rs1632953
rs1632953
HLA-F
1 1.000 0.080 6 29724528 intron variant A/G;T snv 0.700 1.000 1 2007 2007
dbSNP: rs1633069
rs1633069 		1 1.000 0.080 6 29756424 intron variant C/G snv 0.81 0.700 1.000 1 2007 2007
dbSNP: rs1633070
rs1633070 		1 1.000 0.080 6 29756370 intron variant T/A;C snv 0.700 1.000 1 2007 2007
dbSNP: rs1736921
rs1736921
HLA-F ; HLA-F-AS1
1 1.000 0.080 6 29728432 3 prime UTR variant G/A snv 0.82 0.700 1.000 1 2007 2007
dbSNP: rs1737060
rs1737060 		1 1.000 0.080 6 29765192 upstream gene variant G/C snv 0.79 0.700 1.000 1 2007 2007
dbSNP: rs1737068
rs1737068 		1 1.000 0.080 6 29763146 non coding transcript exon variant C/A snv 0.81 0.700 1.000 1 2007 2007
dbSNP: rs17421624
rs17421624
TNXB
2 0.925 0.160 6 32098400 intron variant T/C snv 0.25 0.700 1.000 1 2007 2007
dbSNP: rs17840186
rs17840186
HLA-DMA ; BRD2
1 1.000 0.080 6 32970422 non coding transcript exon variant G/A snv 6.6E-02 0.700 1.000 1 2007 2007
dbSNP: rs1805755
rs1805755
M6PR ; KLRG1
1 1.000 0.080 12 8949816 upstream gene variant A/C;G snv 1.7E-02 0.700 1.000 1 2007 2007
dbSNP: rs184607650
rs184607650
EIF2B4
2 1.000 0.080 2 27367140 missense variant G/C snv 5.1E-04 4.7E-04 0.010 1.000 1 2007 2007
dbSNP: rs2051549
rs2051549
HLA-DQB2
4 0.851 0.280 6 32762309 intron variant G/A snv 0.64 0.700 1.000 1 2007 2007
dbSNP: rs2072633
rs2072633
CFB ; CYP21A2 ; NELFE
6 0.807 0.320 6 31951801 3 prime UTR variant A/G snv 0.59 0.700 1.000 1 2007 2007
dbSNP: rs2073723
rs2073723
TCF19
2 0.925 0.160 6 31162301 intron variant T/C snv 0.78 0.700 1.000 1 2007 2007
dbSNP: rs2076530
rs2076530
BTNL2 ; TSBP1-AS1
17 0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 0.700 1.000 1 2007 2007
dbSNP: rs2076533
rs2076533
BTNL2 ; TSBP1-AS1
3 0.882 0.200 6 32395750 intron variant C/T snv 0.40 0.700 1.000 1 2007 2007
dbSNP: rs2157082
rs2157082 		1 1.000 0.080 6 32792937 intergenic variant G/A;C;T snv 0.700 1.000 1 2007 2007
dbSNP: rs2227127
rs2227127
HLA-DQA2
2 0.925 0.120 6 32744005 intron variant A/G snv 0.37 0.700 1.000 1 2007 2007
dbSNP: rs241403
rs241403
LOC100294145
2 0.925 0.120 6 32899215 downstream gene variant T/C snv 0.52 0.700 1.000 1 2007 2007
dbSNP: rs241427
rs241427
TAP2
2 0.925 0.160 6 32836637 intron variant A/G;T snv 0.700 1.000 1 2007 2007