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 5 2010 2014
dbSNP: rs1421085
rs1421085
FTO
28 0.752 0.280 16 53767042 intron variant T/C snv 0.31 0.700 1.000 4 2009 2014
dbSNP: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.700 1.000 4 2007 2013
dbSNP: rs11671664
rs11671664
GIPR
5 0.925 0.120 19 45669020 intron variant G/A snv 0.12 0.700 1.000 3 2012 2014
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 3 2010 2013
dbSNP: rs17817449
rs17817449
FTO
21 0.716 0.560 16 53779455 intron variant T/A;G snv 0.700 1.000 3 2012 2013
dbSNP: rs2241423
rs2241423
MAP2K5
7 0.882 0.120 15 67794500 intron variant G/A snv 0.29 0.700 1.000 3 2010 2013
dbSNP: rs2815752
rs2815752
LOC105378797
7 0.925 0.200 1 72346757 intron variant G/A snv 0.62 0.700 1.000 3 2009 2013
dbSNP: rs8050136
rs8050136
FTO
32 0.716 0.560 16 53782363 intron variant C/A snv 0.40 0.700 1.000 3 2009 2013
dbSNP: rs987237
rs987237
TFAP2B
10 0.925 0.120 6 50835337 intron variant A/G snv 0.17 0.700 1.000 3 2010 2013
dbSNP: rs10150332
rs10150332
NRXN3
4 14 79470621 intron variant T/C snv 0.26 0.700 1.000 2 2010 2013
dbSNP: rs10767664
rs10767664
BDNF
16 0.752 0.400 11 27704439 intron variant T/A snv 0.83 0.700 1.000 2 2010 2013
dbSNP: rs10968576
rs10968576
LINGO2
10 0.882 0.120 9 28414341 intron variant A/G snv 0.26 0.700 1.000 2 2010 2013
dbSNP: rs11847697
rs11847697
PRKD1
5 14 30045906 intron variant C/T snv 0.13 0.700 1.000 2 2010 2013
dbSNP: rs13078807
rs13078807
CADM2
5 0.925 0.120 3 85835000 intron variant A/G snv 0.15 0.700 1.000 2 2010 2013
dbSNP: rs2030323
rs2030323
BDNF
6 0.925 0.080 11 27706992 intron variant A/C snv 0.83 0.700 1.000 2 2012 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 2013
dbSNP: rs2287019
rs2287019
QPCTL
7 1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 0.700 1.000 2 2010 2013
dbSNP: rs2568958
rs2568958
LOC105378797
8 0.882 0.160 1 72299433 intron variant G/A;C snv 0.700 1.000 2 2009 2013
dbSNP: rs261967
rs261967
LOC101929710 ; LOC107986362
3 5 96514546 intron variant A/C snv 0.42 0.700 1.000 2 2012 2014
dbSNP: rs308971
rs308971
SYN2
3 3 12075120 intron variant G/A snv 0.82 0.800 1.000 2 2012 2012
dbSNP: rs3817334
rs3817334
MTCH2
7 1.000 0.080 11 47629441 intron variant C/T snv 0.36 0.700 1.000 2 2010 2013
dbSNP: rs4771122
rs4771122
MTIF3
4 1.000 0.080 13 27446043 intron variant G/A;C snv 0.700 1.000 2 2010 2013
dbSNP: rs4776970
rs4776970
MAP2K5
4 15 67788548 intron variant A/T snv 0.44 0.700 1.000 2 2012 2014
dbSNP: rs4836133
rs4836133
LINC02240 ; LOC105379158
5 0.925 0.160 5 124996410 intron variant C/A;G;T snv 0.700 1.000 2 2010 2013