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: rs4821544
rs4821544
NCF4 ; NCF4-AS1
6 0.925 0.040 22 36862461 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs5758343
rs5758343 		1 22 41420648 intergenic variant A/T snv 0.82 0.700 1.000 1 2017 2017
dbSNP: rs73205303
rs73205303
RUNX1
1 21 35095533 intron variant G/A snv 9.8E-02 0.700 1.000 1 2017 2017
dbSNP: rs76081789
rs76081789
SIK1
1 21 43426546 intron variant T/C snv 0.700 1.000 1 2017 2017
dbSNP: rs17728960
rs17728960
NFATC2
1 20 51513177 intron variant T/C snv 5.1E-02 0.700 1.000 1 2013 2013
dbSNP: rs17801791
rs17801791
NFATC2
1 20 51522481 intron variant C/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs2766664
rs2766664
LOC101927770
2 1.000 0.080 20 53554702 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2766678
rs2766678
ZNF217
1 20 53591817 intron variant G/A snv 0.86 0.700 1.000 1 2017 2017
dbSNP: rs3208007
rs3208007
RTEL1 ; RTEL1-TNFRSF6B
2 1.000 0.080 20 63690935 synonymous variant T/C;G snv 0.74 0.700 1.000 1 2018 2018
dbSNP: rs3787184
rs3787184
NFATC2
2 1.000 0.120 20 51541298 intron variant A/G snv 0.17 0.700 1.000 1 2017 2017
dbSNP: rs6011033
rs6011033
RTEL1 ; RTEL1-TNFRSF6B
2 20 63691346 intron variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs6021264
rs6021264
NFATC2
1 20 51518144 intron variant A/G snv 6.1E-02 0.700 1.000 1 2013 2013
dbSNP: rs6021268
rs6021268
NFATC2
3 20 51524602 intron variant T/C snv 5.8E-02 0.700 1.000 1 2013 2013
dbSNP: rs6021270
rs6021270
NFATC2
1 20 51524725 intron variant T/C snv 5.7E-02 0.800 1.000 1 2013 2013
dbSNP: rs6096463
rs6096463
NFATC2
1 20 51531498 intron variant G/A snv 5.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs6123048
rs6123048
NFATC2
1 20 51530861 intron variant A/G snv 5.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs6126249
rs6126249
NFATC2
1 20 51526084 intron variant G/A snv 5.7E-02 0.700 1.000 1 2013 2013
dbSNP: rs10414065
rs10414065 		4 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 0.700 1.000 2 2017 2018
dbSNP: rs4574025
rs4574025
TNFRSF11A
4 0.882 0.160 18 62342581 intron variant C/T snv 0.55 0.700 1.000 1 2017 2017
dbSNP: rs4801001
rs4801001 		1 18 54668944 intergenic variant T/C snv 0.62 0.700 1.000 1 2017 2017
dbSNP: rs4795400
rs4795400
GSDMB
3 0.925 0.080 17 39910767 intron variant C/T snv 0.36 0.800 1.000 2 2013 2016
dbSNP: rs869402
rs869402
GSDMB
3 0.925 0.160 17 39911790 intron variant T/A;C snv 0.800 1.000 2 2013 2018
dbSNP: rs1008723
rs1008723
GSDMB
3 0.925 0.160 17 39910014 intron variant G/C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10445308
rs10445308
IKZF3
5 0.851 0.240 17 39781794 intron variant C/T snv 0.38 0.700 1.000 1 2013 2013
dbSNP: rs10852936
rs10852936
ZPBP2
3 0.925 0.120 17 39875461 intron variant C/T snv 0.39 0.40 0.700 1.000 1 2013 2013