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: rs10751647
rs10751647
IFITM2
2 11 306884 upstream gene variant T/C snv 0.49 0.700 1.000 1 2016 2016
dbSNP: rs10956483
rs10956483
CCDC26
3 8 129559864 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs10987830
rs10987830 		2 9 128016459 intergenic variant G/A snv 6.8E-03 0.700 1.000 1 2018 2018
dbSNP: rs1105527
rs1105527
KSR1
2 17 27521170 intron variant C/T snv 0.65 0.700 1.000 1 2016 2016
dbSNP: rs11086102
rs11086102 		6 0.882 19 18287818 upstream gene variant G/C snv 0.64 0.700 1.000 1 2016 2016
dbSNP: rs11189181
rs11189181
RRP12
2 10 97384397 intron variant A/G snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs11190141
rs11190141
NKX2-3 ; LINC01475
3 1.000 0.040 10 99532633 upstream gene variant C/T snv 0.40 0.700 1.000 1 2016 2016
dbSNP: rs112313229
rs112313229 		2 3 46323369 intergenic variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs112505971
rs112505971
ANKRD26
13 10 27068541 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs112721625
rs112721625 		2 17 59850066 upstream gene variant TT/-;T;TTT;TTTT delins 0.700 1.000 1 2016 2016
dbSNP: rs11327184
rs11327184
CCDC26
4 8 129592027 intron variant C/- delins 0.40 0.700 1.000 1 2016 2016
dbSNP: rs113760175
rs113760175
CASC15
3 6 22343363 intron variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs113899791
rs113899791
IRF8
2 16 85902784 5 prime UTR variant GGCTGCAGGT/-;GGCTGCAGGTGGCTGCAGGT;GGCTGCAGGTGGCTGCAGGTGGCTGCAGGT delins 0.700 1.000 1 2016 2016
dbSNP: rs114208039
rs114208039
HLA-B ; HLA-C
2 6 31273862 intron variant A/G snv 0.700 1.000 1 2018 2018
dbSNP: rs115007843
rs115007843
SCD5
2 4 82654059 intron variant A/C snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs115340020
rs115340020
GLMN ; RPAP2
2 1 92300881 intron variant G/A snv 1.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs1157008
rs1157008 		3 9 88920798 regulatory region variant T/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs11580646
rs11580646
TENT5C
2 1 117619797 intron variant C/G snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs11611647
rs11611647 		4 12 4224753 intergenic variant T/C snv 0.22 0.700 1.000 1 2016 2016
dbSNP: rs11640143
rs11640143 		2 16 85955858 regulatory region variant T/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs11642657
rs11642657 		3 16 85982722 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs11686139
rs11686139 		2 2 226426699 intergenic variant A/C snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs11723763
rs11723763
GYPA ; LOC107986317
2 4 144137143 intron variant G/T snv 0.36 0.700 1.000 1 2016 2016
dbSNP: rs117424492
rs117424492 		2 15 79975053 upstream gene variant G/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs117533700
rs117533700
NFIX
2 19 13065914 intron variant C/G;T snv 0.700 1.000 1 2016 2016