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: rs2647044
rs2647044 		3 0.882 0.240 6 32700133 intergenic variant G/A snv 0.10 0.800 1.000 1 2007 2007
dbSNP: rs2664170
rs2664170
GAB3
1 1.000 0.120 X 154717327 intron variant G/A snv 0.800 1.000 1 2009 2009
dbSNP: rs3741208
rs3741208
IGF2 ; IGF2-AS ; INS-IGF2
1 1.000 0.120 11 2148544 non coding transcript exon variant A/G;T snv 0.800 1.000 1 2007 2007
dbSNP: rs3757247
rs3757247
BACH2
5 0.827 0.320 6 90247744 intron variant C/T snv 0.38 0.800 1.000 1 2009 2009
dbSNP: rs3764021
rs3764021
CLEC2D
1 1.000 0.120 12 9681032 splice region variant C/T snv 0.46 0.50 0.800 1.000 1 2007 2007
dbSNP: rs425105
rs425105
PRKD2
2 0.925 0.160 19 46705224 intron variant T/C snv 0.15 0.800 1.000 1 2009 2009
dbSNP: rs4505848
rs4505848
KIAA1109
8 0.776 0.400 4 122211337 intron variant A/G snv 0.29 0.800 1.000 1 2009 2009
dbSNP: rs4763879
rs4763879
CD69
2 0.925 0.160 12 9757568 intron variant G/A snv 0.28 0.800 1.000 1 2009 2009
dbSNP: rs478222
rs478222
EFR3B
1 1.000 0.120 2 25078886 intron variant A/T snv 0.35 0.800 1.000 1 2011 2011
dbSNP: rs4900384
rs4900384 		4 0.882 0.160 14 98032614 intergenic variant A/G snv 0.40 0.800 1.000 1 2009 2009
dbSNP: rs4948088
rs4948088 		2 0.925 0.160 7 50959497 intron variant A/C snv 0.96 0.800 1.000 1 2009 2009
dbSNP: rs539514
rs539514
LMO7
1 1.000 0.120 13 75752146 intron variant A/C;T snv 0.800 1.000 1 2011 2011
dbSNP: rs550448
rs550448
JAZF1-AS1
1 1.000 0.120 7 28189423 intron variant G/A snv 0.86 0.800 1.000 1 2011 2011
dbSNP: rs5753037
rs5753037
HORMAD2 ; LOC105372988
2 0.925 0.160 22 30185733 intron variant C/A;T snv 0.800 1.000 1 2009 2009
dbSNP: rs6547853
rs6547853 		1 1.000 0.120 2 28423934 upstream gene variant G/A snv 0.35 0.800 1.000 1 2011 2011
dbSNP: rs7202877
rs7202877 		3 0.882 0.160 16 75213347 intergenic variant T/C;G snv 0.800 1.000 1 2009 2009
dbSNP: rs7221109
rs7221109 		2 0.925 0.160 17 40614034 intergenic variant T/C snv 0.69 0.800 1.000 1 2009 2009
dbSNP: rs7804356
rs7804356
SKAP2
2 0.925 0.160 7 26852046 intron variant T/C snv 0.21 0.800 1.000 1 2009 2009
dbSNP: rs924043
rs924043 		1 1.000 0.120 6 170063801 regulatory region variant T/C snv 0.71 0.800 1.000 1 2011 2011
dbSNP: rs9268645
rs9268645
HLA-DRA
5 0.827 0.360 6 32440750 intron variant C/G;T snv 0.800 1.000 1 2009 2009
dbSNP: rs9388489
rs9388489
CENPW
2 0.925 0.160 6 126377573 intron variant A/G;T snv 0.800 1.000 1 2009 2009
dbSNP: rs947474
rs947474
LINC02649 ; LINC02656
5 0.827 0.440 10 6348488 intron variant G/A snv 0.79 0.800 1.000 1 2008 2008
dbSNP: rs9976767
rs9976767
UBASH3A
3 0.882 0.200 21 42416281 intron variant A/G snv 0.45 0.800 1.000 1 2009 2009
dbSNP: rs689
rs689
INS ; INS-IGF2
9 0.776 0.280 11 2160994 splice region variant A/T snv 0.73 0.60 0.790 1.000 12 2009 2019
dbSNP: rs706778
rs706778
IL2RA
19 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.750 1.000 6 2007 2015