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: rs10057590
rs10057590
LINC02240
1 5 124999554 intron variant A/C snv 0.62 0.700 1.000 1 2018 2018
dbSNP: rs10171320
rs10171320
LOC101928273
1 2 137928042 intergenic variant A/C snv 0.62 0.700 1.000 1 2018 2018
dbSNP: rs10400054
rs10400054
SORCS3
1 10 105004435 intron variant A/C snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs10510388
rs10510388
LMCD1-AS1
1 3 8215887 intron variant A/C snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs11257952
rs11257952
CAMK1D
1 10 12714714 intron variant A/C snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs1157684
rs1157684 		1 4 133651129 intergenic variant A/C snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs117269860
rs117269860
SLC25A17
1 22 40790485 intron variant A/C snv 2.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs11904541
rs11904541
LOC105374820
1 2 78546010 intergenic variant A/C snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs12376674
rs12376674
LOC105376097
1 9 78872110 TF binding site variant A/C snv 0.10 0.700 1.000 1 2018 2018
dbSNP: rs12739596
rs12739596 		1 1 165390877 intergenic variant A/C snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs12997235
rs12997235
MAPRE3 ; MAPRE3-AS1
1 2 27006211 intron variant A/C snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs17245822
rs17245822 		2 13 72557556 intergenic variant A/C snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs17748359
rs17748359 		1 8 92278935 intergenic variant A/C snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs1993408
rs1993408
LOC107986022
1 3 117892638 intron variant A/C snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs2163503
rs2163503
ZRANB2-AS2
2 1 71335356 intron variant A/C snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs2164552
rs2164552 		1 3 143969456 upstream gene variant A/C snv 0.56 0.700 1.000 1 2018 2018
dbSNP: rs2169642
rs2169642 		1 3 82688622 intergenic variant A/C snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs2239647
rs2239647
AKAP6
7 0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65 0.700 1.000 1 2018 2018
dbSNP: rs2358628
rs2358628
LIN52
1 14 74165054 intron variant A/C snv 0.57 0.700 1.000 1 2018 2018
dbSNP: rs2806934
rs2806934 		1 13 53069972 intergenic variant A/C snv 0.44 0.700 1.000 1 2018 2018
dbSNP: rs2920861
rs2920861
RTN4
1 2 55090980 intron variant A/C snv 0.92 0.700 1.000 1 2018 2018
dbSNP: rs2962438
rs2962438
LOC102723560
1 16 62744695 intergenic variant A/C snv 0.86 0.700 1.000 1 2018 2018
dbSNP: rs317056
rs317056 		1 4 35430215 intergenic variant A/C snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs34088420
rs34088420
CNTNAP2
1 7 146163479 intron variant A/C snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs34116853
rs34116853
LOC105372648
1 20 48877357 regulatory region variant A/C snv 0.32 0.700 1.000 1 2018 2018