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: rs6429432
rs6429432
LINC02768 ; LOC105373215
2 1 235943941 upstream gene variant A/C snv 0.93 0.700 1.000 1 2016 2016
dbSNP: rs413141
rs413141 		4 19 6675978 downstream gene variant A/G snv 0.84 0.700 1.000 1 2016 2016
dbSNP: rs360017
rs360017
LINC01485 ; LOC107986482
2 5 173780350 non coding transcript exon variant A/G snv 0.83 0.700 1.000 1 2016 2016
dbSNP: rs7180079
rs7180079
CSNK1G1
2 15 64337674 intron variant A/G snv 0.79 0.700 1.000 1 2016 2016
dbSNP: rs6540234
rs6540234
LOC105371388
2 16 85949450 downstream gene variant T/C snv 0.78 0.700 1.000 1 2016 2016
dbSNP: rs3731211
rs3731211
CDKN2A
7 9 21986848 intron variant T/A snv 0.74 0.700 1.000 1 2016 2016
dbSNP: rs5875374
rs5875374 		2 6 32459228 downstream gene variant -/AC delins 0.72 0.700 1.000 1 2016 2016
dbSNP: rs865483
rs865483
DUSP14
2 17 37491071 intron variant A/C snv 0.72 0.700 1.000 1 2016 2016
dbSNP: rs7785014
rs7785014 		2 7 138196944 regulatory region variant T/C snv 0.72 0.700 1.000 1 2016 2016
dbSNP: rs35761782
rs35761782
POC1B
2 12 89504600 intron variant -/T delins 0.70 0.700 1.000 1 2016 2016
dbSNP: rs869785
rs869785
THRB
2 3 24306309 intron variant T/C snv 0.70 0.700 1.000 1 2016 2016
dbSNP: rs13022141
rs13022141 		2 2 136131638 intergenic variant A/G snv 0.69 0.700 1.000 1 2016 2016
dbSNP: rs475616
rs475616 		3 10 30207976 regulatory region variant A/G snv 0.67 0.700 1.000 1 2016 2016
dbSNP: rs653178
rs653178
ATXN2
41 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2016 2016
dbSNP: rs12075
rs12075
ACKR1 ; CADM3-AS1
22 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 0.700 1.000 1 2016 2016
dbSNP: rs605783
rs605783
GCNT2
2 6 10526140 intron variant T/A snv 0.65 0.700 1.000 1 2016 2016
dbSNP: rs1105527
rs1105527
KSR1
2 17 27521170 intron variant C/T snv 0.65 0.700 1.000 1 2016 2016
dbSNP: rs4807440
rs4807440
CNN2
3 19 1026478 upstream gene variant G/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: rs66645127
rs66645127
RCBTB1
2 13 49549135 intron variant AAA/-;A;AA;AAAA;AAAAAA delins 0.64 0.700 1.000 1 2016 2016
dbSNP: rs2712381
rs2712381
RPN1
2 3 128619757 downstream gene variant A/C snv 0.61 0.700 1.000 1 2013 2013
dbSNP: rs9554228
rs9554228
FLT3
2 13 28063701 intron variant A/G snv 0.60 0.700 1.000 1 2016 2016
dbSNP: rs2507971
rs2507971
MICB ; MICB-DT
2 6 31493595 intron variant A/T snv 0.59 0.700 1.000 1 2016 2016
dbSNP: rs10276619
rs10276619 		3 1.000 0.080 7 50273756 downstream gene variant G/A snv 0.59 0.700 1.000 1 2018 2018
dbSNP: rs7296503
rs7296503
PDZRN4
13 12 41306962 intron variant C/T snv 0.57 0.700 1.000 1 2019 2019