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: rs9004
rs9004
ZNF7 ; COMMD5
1 8 144842937 stop gained C/G;T snv 1.6E-05; 0.31 0.700 1.000 1 2018 2018
dbSNP: rs157582
rs157582
TOMM40
8 0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 0.700 1.000 1 2017 2017
dbSNP: rs429358
rs429358
APOE
66 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.700 1.000 1 2018 2018
dbSNP: rs6830160
rs6830160
ANAPC4
1 4 25377604 intron variant G/A;T snv 8.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs61751117
rs61751117
RAB11A ; DENND4A
1 15 65741731 synonymous variant A/C snv 2.6E-02 2.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs10058621
rs10058621 		1 5 51259335 intergenic variant T/C snv 6.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs11074779
rs11074779 		1 16 26440122 intergenic variant T/C snv 0.16 0.700 1.000 1 2015 2015
dbSNP: rs11177782
rs11177782
BEST3 ; LOC105369823
1 12 69662005 intron variant C/T snv 1.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs111882035
rs111882035
ARHGAP24
1 4 85495401 intron variant A/G snv 1.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs112108866
rs112108866
CAPN12
1 19 38761240 intron variant C/A;G snv 1.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs11237982
rs11237982 		2 1.000 0.080 11 79730650 intergenic variant T/C snv 0.18 0.700 1.000 1 2015 2015
dbSNP: rs113338984
rs113338984
SNTB2
1 16 69282015 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs116330320
rs116330320
LINC01060
1 4 188507189 intron variant G/A;T snv 3.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs117609474
rs117609474
LINC02331
1 14 53804550 intron variant A/G snv 1.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs11775026
rs11775026
C8orf89
1 8 73264813 intergenic variant T/C snv 5.9E-02 0.700 1.000 1 2017 2017
dbSNP: rs117905930
rs117905930 		2 1.000 0.080 9 88973603 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs118130881
rs118130881
LOC101929492
1 8 31371254 intron variant A/G snv 0.700 1.000 1 2018 2018
dbSNP: rs12268753
rs12268753
PRKG1
1 10 52058389 intron variant A/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs12295181
rs12295181
HBE1 ; HBG2
1 11 5270506 intron variant C/T snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs12436690
rs12436690 		1 14 97119552 intron variant G/A snv 0.12 0.700 1.000 1 2013 2013
dbSNP: rs12990252
rs12990252 		1 2 35861457 intergenic variant G/C snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs13053731
rs13053731
MYH9 ; MIR6819
1 22 36286661 intron variant G/A snv 5.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs13166268
rs13166268 		1 5 121024223 intergenic variant C/G snv 9.2E-02 0.700 1.000 1 2015 2015
dbSNP: rs13360092
rs13360092
LOC107986379
1 5 51233341 intergenic variant G/A snv 6.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs139139710
rs139139710
GALNT17
1 7 71678504 intron variant C/A snv 2.7E-02 0.700 1.000 1 2018 2018