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: rs34823645
rs34823645
C2orf83
1 2 227647210 intron variant T/C snv 3.9E-04 0.700 1.000 1 2019 2019
dbSNP: rs35311980
rs35311980 		1 2 228295484 intergenic variant C/T snv 4.9E-05 0.700 1.000 1 2019 2019
dbSNP: rs35483183
rs35483183
COL4A4
1 2 227011971 intron variant G/A snv 8.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs35924503
rs35924503 		1 2 228266570 intergenic variant T/C snv 1.5E-04 0.700 1.000 1 2018 2018
dbSNP: rs3759794
rs3759794
LTK
1 15 41514460 upstream gene variant G/A snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs4109437
rs4109437
FRG1-DT
1 4 189848068 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs4288924
rs4288924 		1 14 68835682 intergenic variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs4410790
rs4410790
AHR ; LOC101927609
9 0.882 0.160 7 17244953 intron variant T/C snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs4665972
rs4665972
SNX17
9 2 27375230 intron variant T/C snv 0.69 0.700 1.000 1 2018 2018
dbSNP: rs4738817
rs4738817
CHD7
1 8 60708054 intron variant G/A snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs539606836
rs539606836
CUBN
1 10 16963744 intron variant G/A snv 1.7E-04 0.700 1.000 1 2019 2019
dbSNP: rs55798132
rs55798132
LOC105377785
1 8 2808621 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs6535594
rs6535594
NR3C2
2 4 148211605 intron variant G/A snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs6712846
rs6712846 		1 2 207024356 intergenic variant G/A snv 0.53 0.700 1.000 1 2018 2018
dbSNP: rs67339103
rs67339103
LRMDA
2 10 76133928 intron variant G/A;C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs6750228
rs6750228
NRXN1 ; LOC730100
1 2 51084986 intron variant T/A snv 6.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs6768627
rs6768627
MYL3
1 3 46853886 intron variant C/T snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs702634
rs702634
ARL15
3 1.000 0.080 5 53975590 intron variant G/A snv 0.72 0.700 1.000 1 2018 2018
dbSNP: rs7654754
rs7654754
SHROOM3
1 4 76488642 intron variant G/A snv 0.43 0.700 1.000 1 2018 2018
dbSNP: rs7670121
rs7670121
NR3C2
1 4 148207444 intron variant A/G snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs7731168
rs7731168
CWC27
1 5 65000644 intron variant G/C snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs784257
rs784257
LOC105372130
4 1.000 0.080 18 55729968 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs8035855
rs8035855
MAPKBP1
1 15 41785763 intron variant G/A snv 0.59 0.700 1.000 1 2018 2018
dbSNP: rs838142
rs838142
FUT1 ; IZUMO1
1 19 48748894 3 prime UTR variant A/G snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs45551835
rs45551835
CUBN
3 1.000 0.080 10 16890385 missense variant G/A;T snv 1.3E-02; 4.0E-06 0.700 1.000 2 2018 2019