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: rs10980800
rs10980800
LOC105376219
3 9 111153625 intron variant T/C snv 0.21 0.700 1.000 3 2011 2017
dbSNP: rs2124440
rs2124440
ITGA4
2 2 181463487 intron variant G/A snv 0.55 0.700 1.000 3 2013 2017
dbSNP: rs10980797
rs10980797
LOC105376219
3 9 111150273 intron variant A/G;T snv 0.700 1.000 2 2016 2018
dbSNP: rs1892548
rs1892548
LINC00598
2 13 40428504 intron variant T/A;C snv 0.700 1.000 2 2016 2018
dbSNP: rs1991866
rs1991866
CCDC26
3 8 129611859 intron variant G/A;C snv 0.700 1.000 2 2014 2017
dbSNP: rs3095254
rs3095254 		3 6 31253891 intergenic variant C/A;G snv 0.55 0.700 1.000 2 2011 2014
dbSNP: rs445
rs445
CDK6
9 7 92779056 intron variant C/T snv 0.14 0.700 1.000 2 2016 2018
dbSNP: rs4970966
rs4970966
ENSA
2 1 150611627 intron variant G/T snv 0.16 0.700 1.000 2 2016 2018
dbSNP: rs10098310
rs10098310
CCDC26
3 8 129601368 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10147992
rs10147992
STXBP6
3 14 25034593 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10168795
rs10168795
DOCK10
2 2 224888625 intron variant A/G snv 0.24 0.700 1.000 1 2016 2016
dbSNP: rs1021479
rs1021479 		2 16 85923808 upstream gene variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs1037171
rs1037171
CD300LF ; RAB37
2 17 74706839 intron variant G/A snv 0.53 0.700 1.000 1 2016 2016
dbSNP: rs10418046
rs10418046
NLRP12
3 19 53824615 upstream gene variant T/G snv 0.26 0.700 1.000 1 2016 2016
dbSNP: rs1042133
rs1042133
HLA-DPA1 ; HLA-DPB1
2 6 33080829 missense variant G/C snv 0.14 0.15 0.700 1.000 1 2016 2016
dbSNP: rs10489481
rs10489481 		2 1 185422035 regulatory region variant G/A snv 0.31 0.700 1.000 1 2016 2016
dbSNP: rs10562650
rs10562650
ITGA4
2 2 181459460 intron variant TT/-;T;TTT delins 0.56 0.700 1.000 1 2016 2016
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: rs11189181
rs11189181
RRP12
2 10 97384397 intron variant A/G snv 0.30 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