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: rs10059884
rs10059884 		5 5 32832368 regulatory region variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10255839
rs10255839
EVX1
6 7 27249498 intron variant G/A snv 0.87 0.700 1.000 1 2018 2018
dbSNP: rs10743353
rs10743353
LINC02398
2 12 20047028 intron variant C/T snv 0.60 0.700 1.000 1 2018 2018
dbSNP: rs11065979
rs11065979 		12 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs11099097
rs11099097 		6 4 80246155 intergenic variant C/T snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs11725969
rs11725969
GUCY1A1
5 4 155705436 intron variant C/T snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs1275986
rs1275986 		2 2 26689211 upstream gene variant C/A snv 0.50 0.700 1.000 1 2018 2018
dbSNP: rs1290784
rs1290784
MECOM
6 3 169379112 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs13306556
rs13306556
MTHFR
2 1 11792053 intron variant C/T snv 0.10 0.700 1.000 1 2018 2018
dbSNP: rs1350193
rs1350193
CSK
2 15 74791940 intron variant G/C snv 0.67 0.700 1.000 1 2018 2018
dbSNP: rs1579381
rs1579381 		2 12 115118002 intergenic variant C/G snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs1689040
rs1689040 		4 12 89584456 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs17035646
rs17035646
CASZ1
6 1 10736490 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1801253
rs1801253
ADRB1
34 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.700 1.000 1 2018 2018
dbSNP: rs1894400
rs1894400
FES
5 15 90885725 intron variant C/T snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs1980235
rs1980235
LOC107984543
2 12 89717005 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs198851
rs198851
H4C3
15 6 26104404 downstream gene variant T/A;C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs2013002
rs2013002 		5 12 111762346 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs2306363
rs2306363
SIPA1
7 11 65638129 5 prime UTR variant G/T snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs3753584
rs3753584
CLCN6 ; MTHFR
10 0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs3792765
rs3792765
NPR3
2 5 32713730 intron variant A/G snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs438885
rs438885 		5 2 164195781 intron variant A/T snv 0.56 0.700 1.000 1 2018 2018
dbSNP: rs5883070
rs5883070 		5 7 27240226 intron variant -/AAAACA;AACA delins 0.91 0.700 1.000 1 2018 2018
dbSNP: rs604723
rs604723
ARHGAP42
9 1.000 0.040 11 100739815 intron variant T/C snv 0.78 0.700 1.000 1 2018 2018
dbSNP: rs6108787
rs6108787 		5 20 10986566 intron variant T/G snv 0.46 0.700 1.000 1 2018 2018