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: rs1001096
rs1001096
ART4 ; C12orf60
1 12 14835521 intron variant G/A snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs10023470
rs10023470
SORCS2 ; PSAPL1
1 4 7432729 3 prime UTR variant A/G snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs10030035
rs10030035
NUDT9
1 4 87430452 intron variant T/C snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs10030217
rs10030217
UNC5C
1 4 95536653 intron variant T/A snv 0.64 0.700 1.000 1 2018 2018
dbSNP: rs10031452
rs10031452
CXCL9 ; LOC101928809
1 4 76003780 intron variant T/C snv 0.62 0.700 1.000 1 2018 2018
dbSNP: rs10033900
rs10033900
CFI
7 0.807 0.040 4 109737911 intron variant T/C snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs10038416
rs10038416
SPINK6
1 5 148213668 intron variant A/G snv 0.78 0.700 1.000 1 2018 2018
dbSNP: rs10055396
rs10055396 		1 5 148182067 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1005636
rs1005636 		1 19 43302407 downstream gene variant T/C snv 0.88 0.700 1.000 1 2018 2018
dbSNP: rs10094645
rs10094645
TTI2
1 8 33502689 intron variant G/A snv 0.53 0.700 1.000 1 2018 2018
dbSNP: rs1011063
rs1011063
NISCH
1 3 52472832 intron variant C/T snv 0.81 0.700 1.000 1 2018 2018
dbSNP: rs10117466
rs10117466
FCN1
1 9 134918015 upstream gene variant G/T snv 0.25 0.700 1.000 1 2018 2018
dbSNP: rs10128781
rs10128781
ERGIC2
1 12 29367773 intron variant T/C snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs1013579
rs1013579
C8B
1 1 56956811 missense variant C/T snv 0.98 0.98 0.700 1.000 1 2018 2018
dbSNP: rs10136766
rs10136766
IGHG3 ; LOC105378184
1 14 105766248 intron variant A/G snv 0.49 0.700 1.000 1 2018 2018
dbSNP: rs10139058
rs10139058 		1 14 106685899 upstream gene variant C/T snv 0.42 0.700 1.000 1 2018 2018
dbSNP: rs10139745
rs10139745
SERPINA5 ; SERPINA4
1 14 94569037 intron variant G/A snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs10144381
rs10144381 		1 14 100706960 regulatory region variant C/A;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10146582
rs10146582
SERPINA5
1 14 94571441 intron variant G/A snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs10149354
rs10149354
SERPINA5
1 14 94572031 intron variant C/T snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs1015456
rs1015456
LOC105376921 ; LOC107986040
1 3 66093 intergenic variant T/C snv 0.43 0.700 1.000 1 2018 2018
dbSNP: rs10159712
rs10159712
PLXDC2
1 10 19971440 intron variant G/A snv 0.74 0.700 1.000 1 2018 2018
dbSNP: rs10179654
rs10179654 		1 2 102305323 regulatory region variant T/G snv 0.55 0.700 1.000 1 2018 2018
dbSNP: rs1018454
rs1018454
DPT
1 1 168728523 intron variant A/C snv 0.57 0.700 1.000 2 2018 2018
dbSNP: rs1019016
rs1019016 		1 7 80941246 regulatory region variant G/T snv 0.53 0.700 1.000 1 2018 2018