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: rs1558902
rs1558902
FTO
21 0.827 0.120 16 53769662 intron variant T/A snv 0.31 0.700 1.000 11 2010 2019
dbSNP: rs3810291
rs3810291
ZC3H4
9 19 47065746 3 prime UTR variant G/A snv 0.50 0.700 1.000 10 2010 2019
dbSNP: rs2112347
rs2112347
POC5 ; LOC441087
10 0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 0.700 1.000 9 2010 2019
dbSNP: rs3817334
rs3817334
MTCH2
7 1.000 0.080 11 47629441 intron variant C/T snv 0.36 0.700 1.000 8 2010 2018
dbSNP: rs10968576
rs10968576
LINGO2
10 0.882 0.120 9 28414341 intron variant A/G snv 0.26 0.700 1.000 5 2010 2018
dbSNP: rs2287019
rs2287019
QPCTL
7 1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 0.700 1.000 5 2010 2018
dbSNP: rs987237
rs987237
TFAP2B
10 0.925 0.120 6 50835337 intron variant A/G snv 0.17 0.700 1.000 5 2010 2019
dbSNP: rs11847697
rs11847697
PRKD1
5 14 30045906 intron variant C/T snv 0.13 0.700 1.000 4 2010 2018
dbSNP: rs2241423
rs2241423
MAP2K5
7 0.882 0.120 15 67794500 intron variant G/A snv 0.29 0.700 1.000 4 2010 2019
dbSNP: rs2867125
rs2867125 		8 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 0.700 1.000 4 2010 2019
dbSNP: rs2890652
rs2890652 		3 2 142202362 intergenic variant T/C snv 0.21 0.700 1.000 3 2010 2018
dbSNP: rs571312
rs571312 		7 1.000 0.080 18 60172536 intergenic variant C/A snv 0.26 0.700 1.000 3 2010 2017
dbSNP: rs713586
rs713586 		5 0.925 0.160 2 24935139 intergenic variant T/C snv 0.58 0.700 1.000 3 2010 2019
dbSNP: rs887912
rs887912 		6 1.000 0.080 2 59075742 intron variant T/C;G snv 0.700 1.000 3 2010 2019
dbSNP: rs9816226
rs9816226
DGKG
5 1.000 0.080 3 186116710 intron variant A/T snv 0.82 0.700 1.000 3 2010 2019
dbSNP: rs10150332
rs10150332
NRXN3
4 14 79470621 intron variant T/C snv 0.26 0.700 1.000 2 2010 2019
dbSNP: rs10767664
rs10767664
BDNF
16 0.752 0.400 11 27704439 intron variant T/A snv 0.83 0.700 1.000 2 2010 2019
dbSNP: rs1514175
rs1514175
TNNI3K ; FPGT-TNNI3K ; LRRC53
4 1.000 0.080 1 74525960 intron variant A/G snv 0.48 0.700 1.000 2 2010 2013
dbSNP: rs206936
rs206936
NUDT3 ; RPS10-NUDT3
8 0.882 0.160 6 34335092 intron variant A/G snv 0.34 0.700 1.000 2 2010 2018
dbSNP: rs10458787
rs10458787 		4 1.000 0.040 10 4613373 intergenic variant A/C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs12444979
rs12444979
LOC105371116
4 1.000 0.080 16 19922278 intergenic variant C/T snv 0.11 0.700 1.000 1 2010 2010
dbSNP: rs13078807
rs13078807
CADM2
5 0.925 0.120 3 85835000 intron variant A/G snv 0.15 0.700 1.000 1 2010 2010
dbSNP: rs1555543
rs1555543 		3 1 96479241 intergenic variant A/C snv 0.55 0.700 1.000 1 2010 2010
dbSNP: rs2275215
rs2275215
LOC102723409
3 6 129540247 intron variant T/C snv 0.35 0.700 1.000 1 2010 2010
dbSNP: rs2444217
rs2444217
ADCY9
3 16 3988386 intron variant G/A snv 0.45 0.700 1.000 1 2010 2010