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: rs1990760
rs1990760
IFIH1
33 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 0.700 1.000 1 2010 2010
dbSNP: rs2187668
rs2187668
HLA-DQA1 ; HLA-DQA2 ; LOC107986589
20 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.700 1.000 1 2010 2010
dbSNP: rs2280401
rs2280401
RPS11 ; SNORD35B
5 19 49496752 intron variant G/A snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs4273077
rs4273077
TNFRSF13B
4 0.925 0.160 17 16945825 intron variant A/G snv 0.13 0.700 1.000 1 2010 2010
dbSNP: rs6498142
rs6498142
CLEC16A
3 16 10987392 intron variant C/G snv 0.77 0.700 1.000 1 2010 2010
dbSNP: rs669408
rs669408 		2 1 232383404 regulatory region variant A/C snv 0.52 0.700 1.000 1 2010 2010
dbSNP: rs9271366
rs9271366 		9 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 0.700 1.000 1 2010 2010
dbSNP: rs1002054
rs1002054
MAPK1IP1L
1 14 55062195 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1009647
rs1009647
ATG14
2 1.000 0.120 14 55413329 upstream gene variant G/A snv 0.24 0.700 1.000 1 2012 2012
dbSNP: rs1009648
rs1009648
ATG14
1 14 55413451 upstream gene variant T/C snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs1009714
rs1009714
KTN1-AS1
1 14 55512820 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1009977
rs1009977
LGALS3
2 1.000 0.040 14 55136284 intron variant T/G snv 0.48 0.700 1.000 1 2012 2012
dbSNP: rs1009978
rs1009978
LGALS3
1 14 55136343 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10129505
rs10129505
FBXO34
1 14 55309657 intron variant C/T snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs10130783
rs10130783 		1 14 55714800 intergenic variant G/A snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs10131232
rs10131232
GCH1
1 14 54849190 intron variant G/A snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs10131730
rs10131730
ATG14
1 14 55373374 intron variant C/T snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs10133662
rs10133662
GCH1
1 14 54849552 intron variant A/G snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs10134019
rs10134019
KTN1-AS1
1 14 55530274 intron variant T/G snv 0.54 0.700 1.000 1 2012 2012
dbSNP: rs10134317
rs10134317
FBXO34
1 14 55326730 intron variant C/A;G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10134339
rs10134339
FBXO34
1 14 55347662 intron variant T/C snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs10134800
rs10134800
DLGAP5
1 14 55168491 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10134983
rs10134983
DLGAP5
1 14 55168605 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10135789
rs10135789 		1 14 54825302 intergenic variant A/G snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs10136596
rs10136596
ATG14
1 14 55370055 intron variant A/G;T snv 0.700 1.000 1 2012 2012