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: rs6048205
rs6048205
LINC00261
3 1.000 0.080 20 22578963 upstream gene variant A/G snv 9.1E-02 0.800 1.000 1 2012 2012
dbSNP: rs7034200
rs7034200
GLIS3
3 1.000 0.080 9 4289050 intron variant C/A;G snv 0.800 1.000 1 2012 2012
dbSNP: rs7173964
rs7173964 		3 1.000 0.080 15 62104743 regulatory region variant G/A snv 0.49 0.800 1.000 1 2012 2012
dbSNP: rs7944584
rs7944584
MADD
5 1.000 0.080 11 47314769 intron variant A/T snv 0.19 0.800 1.000 1 2012 2012
dbSNP: rs10938397
rs10938397 		19 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 0.700 1.000 14 2009 2019
dbSNP: rs543874
rs543874 		11 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 0.700 1.000 14 2010 2019
dbSNP: rs6567160
rs6567160 		12 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 0.700 1.000 12 2014 2019
dbSNP: rs7138803
rs7138803 		17 0.827 0.240 12 49853685 intergenic variant G/A;T snv 0.700 1.000 12 2009 2019
dbSNP: rs13107325
rs13107325
SLC39A8
34 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 0.700 1.000 11 2010 2019
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: rs12429545
rs12429545 		4 13 53528071 intron variant G/A;T snv 0.12 0.700 1.000 10 2015 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: rs10182181
rs10182181 		3 1.000 0.080 2 24927427 intergenic variant A/G snv 0.57 0.700 1.000 8 2015 2019
dbSNP: rs13021737
rs13021737 		2 2 632348 intergenic variant A/G snv 0.85 0.700 1.000 8 2015 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: rs10132280
rs10132280 		6 14 25458973 intergenic variant C/A snv 0.37 0.700 1.000 7 2015 2019
dbSNP: rs12446632
rs12446632
LOC105371116
7 1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 0.700 1.000 7 2015 2019
dbSNP: rs1516725
rs1516725
DGKG ; ETV5
8 0.925 0.120 3 186106215 intron variant T/C snv 0.86 0.700 1.000 7 2013 2019
dbSNP: rs17024393
rs17024393
GNAT2
4 1 109612066 intron variant T/C snv 4.6E-02 0.700 1.000 7 2015 2019
dbSNP: rs17405819
rs17405819 		3 8 75894349 intergenic variant T/C snv 0.24 0.700 1.000 7 2015 2019
dbSNP: rs1928295
rs1928295 		3 9 117616205 intergenic variant T/C snv 0.45 0.700 1.000 7 2015 2019
dbSNP: rs2365389
rs2365389
FHIT
3 3 61250788 intron variant C/T snv 0.56 0.700 1.000 7 2015 2018
dbSNP: rs3101336
rs3101336
LOC105378797
6 1.000 0.080 1 72285502 intron variant T/C snv 0.62 0.700 1.000 7 2015 2019
dbSNP: rs6265
rs6265
BDNF ; BDNF-AS
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.700 1.000 7 2009 2019