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: rs12979278
rs12979278
MAMSTR
9 0.790 0.080 19 48715345 synonymous variant C/T snv 0.46 0.40 0.700 1.000 1 2019 2019
dbSNP: rs13020391
rs13020391
PNKD ; LOC105373881
9 0.790 0.080 2 218319713 intron variant C/T snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs13086367
rs13086367 		10 0.776 0.080 3 113185041 downstream gene variant A/G snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs13149359
rs13149359 		10 0.776 0.080 4 94017467 intergenic variant C/A snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs13204733
rs13204733 		10 0.776 0.080 6 55701310 intergenic variant A/G snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs1321310
rs1321310 		9 0.790 0.080 6 36655347 regulatory region variant T/C snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs1330889
rs1330889
LINC00446 ; OBI1-AS1
9 0.790 0.080 13 78035480 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs13831
rs13831
GNAS
9 0.790 0.080 20 58900136 3 prime UTR variant A/G snv 0.77 0.700 1.000 1 2019 2019
dbSNP: rs1391441
rs1391441
TET2 ; TET2-AS1
11 0.763 0.240 4 105207603 intron variant G/A snv 0.70 0.700 1.000 1 2019 2019
dbSNP: rs1412834
rs1412834
CDKN2B-AS1
11 0.790 0.080 9 22110132 intron variant T/C snv 0.64 0.700 1.000 1 2019 2019
dbSNP: rs1427760
rs1427760 		10 0.776 0.080 12 114662909 upstream gene variant T/C snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs1445011
rs1445011 		9 0.790 0.080 5 40280100 intergenic variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs145364999
rs145364999
CHD1
10 0.776 0.080 5 98870378 intron variant T/A snv 1.9E-03 0.700 1.000 1 2019 2019
dbSNP: rs1476570
rs1476570 		9 0.790 0.080 6 29842083 intergenic variant G/A;T snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs1535
rs1535
FADS2
24 0.752 0.240 11 61830500 intron variant A/G snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs1537372
rs1537372
CDKN2B-AS1
14 0.752 0.120 9 22103184 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1570405
rs1570405
LOC105370507
9 0.790 0.080 14 54087516 regulatory region variant G/A snv 0.55 0.700 1.000 1 2019 2019
dbSNP: rs16959063
rs16959063
FMN1 ; LOC107984089
9 0.790 0.080 15 32813529 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs17011141
rs17011141
LINC02257
10 0.776 0.080 1 221939292 intron variant A/G snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs17035289
rs17035289 		9 0.790 0.080 4 105127134 intergenic variant T/C snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs174533
rs174533
MYRF ; TMEM258
18 0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 0.700 1.000 1 2019 2019
dbSNP: rs1886450
rs1886450 		9 0.790 0.080 13 73412491 upstream gene variant A/G snv 0.65 0.700 1.000 1 2019 2019
dbSNP: rs189583
rs189583 		10 0.776 0.080 20 6395810 regulatory region variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1924816
rs1924816 		10 0.776 0.080 13 73423824 intron variant A/G snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs1963413
rs1963413
B9D2 ; TMEM91
10 0.776 0.080 19 41365668 intron variant G/A;C;T snv 0.700 1.000 1 2019 2019