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: rs113569514
rs113569514
SLCO2A1
9 0.790 0.080 3 134029945 intron variant T/C snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs114436839
rs114436839
PLCH1
9 0.790 0.080 3 155691561 intron variant G/A snv 1.8E-03 0.700 1.000 1 2018 2018
dbSNP: rs115392158
rs115392158
HLA-B
17 0.708 0.280 6 31347004 intron variant A/G snv 0.700 1.000 1 2016 2016
dbSNP: rs115707823
rs115707823 		19 0.701 0.320 6 30374976 intergenic variant G/A snv 0.700 1.000 1 2016 2016
dbSNP: rs11571818
rs11571818
BRCA2
17 0.708 0.280 13 32394673 intron variant T/C snv 6.6E-03 6.0E-03 0.700 1.000 1 2016 2016
dbSNP: rs11571833
rs11571833
BRCA2
43 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 0.700 1.000 1 2016 2016
dbSNP: rs11610543
rs11610543 		10 0.776 0.080 12 42740389 intergenic variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs116353863
rs116353863 		10 0.776 0.080 6 31042408 regulatory region variant T/C snv 2.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs11692435
rs11692435
ACTR1B
10 0.790 0.080 2 97658891 missense variant G/A snv 7.0E-02 6.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs117079142
rs117079142
UTP23 ; LOC112268030
10 0.776 0.080 8 116778675 intron variant C/A snv 3.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs11727676
rs11727676
HHIP
14 0.776 0.080 4 144737912 synonymous variant T/C snv 6.6E-02 6.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs11844632
rs11844632
RAD51B
17 0.708 0.280 14 68559662 intron variant G/A snv 0.23 0.700 1.000 1 2016 2016
dbSNP: rs11884596
rs11884596
LOC105373831
10 0.776 0.080 2 198747683 intron variant T/C snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs11893063
rs11893063
LOC105373831
9 0.790 0.080 2 198737201 intron variant G/A snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs11903757
rs11903757 		11 0.763 0.160 2 191722478 intron variant T/C snv 0.16 0.700 1.000 1 2013 2013
dbSNP: rs11907546
rs11907546 		17 0.708 0.280 20 34131991 upstream gene variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs11927424
rs11927424 		9 0.790 0.080 3 88708681 intergenic variant A/G snv 0.39 0.700 1.000 1 2017 2017
dbSNP: rs12143541
rs12143541
TTC22
9 0.790 0.080 1 54782179 intron variant A/G snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs12144319
rs12144319
TTC22
10 0.776 0.080 1 54780362 3 prime UTR variant T/C snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs12149163
rs12149163 		10 0.776 0.080 16 86305709 upstream gene variant T/C snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs12246635
rs12246635
VTI1A
10 0.776 0.080 10 112528860 intron variant T/C snv 0.13 0.700 1.000 1 2019 2019
dbSNP: rs12255141
rs12255141
VTI1A
9 0.790 0.080 10 112535133 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs12372718
rs12372718
ATF1
10 0.776 0.080 12 50777307 intron variant A/G snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs12427600
rs12427600
SMAD9
9 0.790 0.080 13 36886511 intron variant T/C snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs12447408
rs12447408 		10 0.776 0.080 16 86218938 downstream gene variant G/A snv 0.21 0.700 1.000 1 2019 2019