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: rs1149833
rs1149833
DLEU1
2 0.925 0.160 13 50176740 intron variant A/T snv 0.47 0.700 1.000 1 2019 2019
dbSNP: rs11706588
rs11706588
CHCHD6
2 0.925 0.160 3 126729670 intron variant T/C snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs117482282
rs117482282 		2 0.925 0.160 6 165097982 intergenic variant C/T snv 3.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs12629668
rs12629668
ZIC1 ; LOC440982
2 0.925 0.160 3 147491392 intron variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs140306040
rs140306040 		2 0.925 0.160 7 62860773 intergenic variant C/T snv 0.700 1.000 1 2019 2019
dbSNP: rs1406230
rs1406230
ALK
2 0.925 0.160 2 29360455 intron variant C/T snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs34954281
rs34954281
TNFAIP6 ; MIR4773-2 ; LOC101929319
2 0.925 0.160 2 151369363 intron variant C/T snv 0.22 0.700 1.000 1 2019 2019
dbSNP: rs35498131
rs35498131 		2 0.925 0.160 16 9026952 intergenic variant A/G snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs3818329
rs3818329
RGS13
2 0.925 0.160 1 192658630 non coding transcript exon variant G/A snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs9966620
rs9966620
TTC39C
2 0.925 0.160 18 24100771 intron variant G/A snv 0.21 0.700 1.000 1 2019 2019