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: rs150491901
rs150491901 		1 1.000 0.040 8 10468395 intergenic variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1539844
rs1539844
CELF4
1 1.000 0.040 18 37540169 intron variant G/A snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs16902946
rs16902946 		1 1.000 0.040 5 87982999 intron variant T/C snv 0.22 0.700 1.000 1 2018 2018
dbSNP: rs17196295
rs17196295
SATB2
1 1.000 0.040 2 199287475 intron variant A/G snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs1724725
rs1724725
RSRC1
1 1.000 0.040 3 158184607 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs17532098
rs17532098
FAM120A
1 1.000 0.040 9 93500443 intron variant C/T snv 7.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs1826787
rs1826787 		1 1.000 0.040 10 105908635 downstream gene variant C/T snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs1890184
rs1890184
CNNM2
1 1.000 0.040 10 102988702 intron variant A/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1938386
rs1938386
COQ8A ; LOC107985354
1 1.000 0.040 1 226909338 intron variant G/T snv 0.57 0.700 1.000 1 2018 2018
dbSNP: rs1998122
rs1998122
DTD1
1 1.000 0.040 20 18727895 intron variant G/A snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs2194027
rs2194027
LINC00461
1 1.000 0.040 5 88526854 intron variant T/A snv 0.37 0.700 1.000 1 2018 2018
dbSNP: rs2236939
rs2236939
SLC38A3
1 1.000 0.040 3 50206077 intron variant G/T snv 0.10 0.700 1.000 1 2018 2018
dbSNP: rs2407746
rs2407746 		1 1.000 0.040 8 5080235 regulatory region variant C/G snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs2413631
rs2413631
RBX1
1 1.000 0.040 22 40963782 intron variant G/A snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs2435210
rs2435210
MAPT
1 1.000 0.040 17 45984528 intron variant C/T snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs246914
rs246914 		1 1.000 0.040 5 103223706 intergenic variant T/C snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs2488401
rs2488401
DENND1B
1 1.000 0.040 1 197733271 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2672852
rs2672852 		1 1.000 0.040 2 103455652 intergenic variant C/T snv 0.44 0.700 1.000 1 2018 2018
dbSNP: rs28426374
rs28426374
DLST
1 1.000 0.040 14 74880037 upstream gene variant C/T snv 0.51 0.700 1.000 1 2018 2018
dbSNP: rs28639817
rs28639817
SGCZ
1 1.000 0.040 8 14293898 intron variant A/G snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs3117425
rs3117425
LOC105375005
1 1.000 0.040 6 29292654 non coding transcript exon variant C/T snv 8.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs3124377
rs3124377 		1 1.000 0.040 13 55411477 intergenic variant C/T snv 0.63 0.700 1.000 1 2018 2018
dbSNP: rs3213716
rs3213716
RPS6KL1
1 1.000 0.040 14 74911482 non coding transcript exon variant G/A snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs332828
rs332828
NFIA
1 1.000 0.040 1 61277021 intron variant G/A snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs34011394
rs34011394
ZC3H7B
1 1.000 0.040 22 41308868 intron variant C/T snv 0.38 0.700 1.000 1 2018 2018