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: rs11087784
rs11087784 		10 0.776 0.080 20 7760329 intergenic variant A/G snv 0.13 0.700 1.000 1 2019 2019
dbSNP: rs11119608
rs11119608
KCNH1
17 0.708 0.280 1 210816167 intron variant T/G snv 0.21 0.700 1.000 1 2016 2016
dbSNP: rs11150038
rs11150038
CLEC3A
10 0.790 0.080 16 78042662 intron variant A/C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs11168936
rs11168936
TUBA1C
17 0.708 0.280 12 49251457 intron variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs11169552
rs11169552
ATF1
10 0.776 0.080 12 50761880 upstream gene variant C/T snv 0.23 0.700 1.000 1 2010 2010
dbSNP: rs11169572
rs11169572 		9 0.790 0.080 12 50823107 downstream gene variant T/C snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs11190164
rs11190164 		10 0.776 0.080 10 99591947 intergenic variant A/G snv 0.19 0.700 1.000 3 2015 2019
dbSNP: rs11196170
rs11196170
TCF7L2
10 0.776 0.080 10 112962862 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs11196172
rs11196172
TCF7L2
18 0.708 0.200 10 112967084 intron variant G/A snv 0.13 0.700 1.000 4 2014 2019
dbSNP: rs11200014
rs11200014
FGFR2
19 0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 0.700 1.000 1 2016 2016
dbSNP: rs11255841
rs11255841 		11 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 0.700 1.000 5 2014 2019
dbSNP: rs113488022
rs113488022
BRAF
490 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.020 1.000 2 2013 2018
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: rs1143634
rs1143634
IL1B
52 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 0.010 1.000 1 2018 2018
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: rs11571658
rs11571658
BRCA2
6 0.851 0.240 13 32340630 frameshift variant TT/- del 2.8E-05 0.700 0
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