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: rs10521261
rs10521261
CASC22 ; LOC105371261
1 1.000 0.040 16 52266343 intron variant T/G snv 0.15 0.700 1.000 1 2016 2016
dbSNP: rs1053544
rs1053544
REV1
1 1.000 0.040 2 99405808 non coding transcript exon variant G/A snv 0.43 0.700 1.000 1 2013 2013
dbSNP: rs1055447
rs1055447
C11orf49 ; ARFGAP2
2 1.000 0.040 11 47164873 3 prime UTR variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1058172
rs1058172
CYP2D6 ; NDUFA6-DT
4 0.882 0.080 22 42127526 missense variant C/G;T snv 4.4E-06; 9.2E-02 0.700 1.000 1 2014 2014
dbSNP: rs1061170
rs1061170
CFH
72 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2016 2016
dbSNP: rs1064346
rs1064346
OSTM1
1 1.000 0.040 6 108043747 3 prime UTR variant T/C snv 0.25 0.700 1.000 1 2017 2017
dbSNP: rs1065852
rs1065852
CYP2D6 ; NDUFA6-DT ; LOC112268294
19 0.695 0.360 22 42130692 missense variant G/A snv 0.21 0.19 0.700 1.000 1 2014 2014
dbSNP: rs10736648
rs10736648
GRIA4
1 1.000 0.040 11 105772210 intron variant A/G snv 0.56 0.010 1.000 1 2013 2013
dbSNP: rs1074145
rs1074145 		2 1.000 0.040 10 94922089 intergenic variant G/A snv 0.16 0.700 1.000 1 2014 2014
dbSNP: rs10744560
rs10744560
CACNA1C ; CACNA1C-IT3
3 0.882 0.040 12 2277933 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10748045
rs10748045
GRIP1
3 0.925 0.040 12 66422359 intron variant A/G snv 0.41 0.700 1.000 1 2014 2014
dbSNP: rs10748842
rs10748842
NRG3
8 0.807 0.120 10 81889983 intron variant T/C snv 0.13 0.010 1.000 1 2017 2017
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
44 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.700 1.000 1 2013 2013
dbSNP: rs10762080
rs10762080
CTNNA3
1 1.000 0.040 10 66637687 intron variant A/G snv 0.67 0.700 1.000 1 2018 2018
dbSNP: rs10767735
rs10767735
LINC02758
1 1.000 0.040 11 28621014 regulatory region variant G/A;C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10769025
rs10769025
ALX4
3 0.882 0.160 11 44267885 intron variant G/C snv 0.58 0.700 1.000 1 2018 2018
dbSNP: rs10774035
rs10774035
CACNA1C
2 0.925 0.040 12 2259508 intron variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10774036
rs10774036
CACNA1C ; CACNA1C-IT3
1 1.000 0.040 12 2277782 intron variant C/T snv 0.25 0.700 1.000 1 2011 2011
dbSNP: rs10774037
rs10774037
CACNA1C
3 0.882 0.040 12 2311360 intron variant G/A snv 0.77 0.800 1.000 2 2013 2019
dbSNP: rs10780035
rs10780035
NEK4
1 1.000 0.040 3 52730608 intron variant C/T snv 0.34 0.700 1.000 1 2013 2013
dbSNP: rs10786831
rs10786831
SORCS3
1 1.000 0.040 10 104854813 intron variant A/G snv 0.50 0.700 1.000 1 2016 2016
dbSNP: rs10789214
rs10789214
SGIP1
1 1.000 0.040 1 66681134 intron variant C/T snv 0.67 0.700 1.000 1 2019 2019
dbSNP: rs10789340
rs10789340
LOC105378797
2 0.925 0.120 1 72474590 intron variant A/G;T snv 0.700 1.000 2 2018 2019
dbSNP: rs10795187
rs10795187 		1 1.000 0.040 10 4567598 intergenic variant G/A snv 0.28 0.700 1.000 1 2017 2017
dbSNP: rs10809385
rs10809385 		1 1.000 0.040 9 11208995 intergenic variant C/A;T snv 0.700 1.000 1 2018 2018