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: rs12429545
rs12429545 		4 13 53528071 intron variant G/A;T snv 0.12 0.700 1.000 10 2015 2019
dbSNP: rs7903146
rs7903146
TCF7L2
93 0.554 0.680 10 112998590 intron variant C/G;T snv 0.800 1.000 9 2012 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: 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: 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: rs6864049
rs6864049
LINC02240 ; LOC105379158
2 5 124994829 intron variant A/C;G;T snv 0.700 1.000 7 2015 2019
dbSNP: rs11030104
rs11030104
BDNF ; BDNF-AS
12 0.790 0.240 11 27662970 intron variant A/G snv 0.16 0.700 1.000 6 2014 2019
dbSNP: rs13191362
rs13191362
PRKN
3 6 162612318 intron variant A/G snv 8.7E-02 0.700 1.000 6 2015 2019
dbSNP: rs16851483
rs16851483
RASA2
4 0.925 0.080 3 141556594 intron variant G/T snv 6.7E-02 0.700 1.000 6 2015 2019
dbSNP: rs16907751
rs16907751 		1 8 80463222 intron variant C/T snv 0.10 0.700 1.000 6 2015 2019
dbSNP: rs2033529
rs2033529
TDRG1
4 6 40380914 intron variant A/C;G snv 0.700 1.000 6 2015 2019
dbSNP: rs7124681
rs7124681
CELF1
2 11 47508395 intron variant C/A snv 0.36 0.700 1.000 6 2015 2019
dbSNP: rs7141420
rs7141420
NRXN3
5 1.000 0.080 14 79433111 intron variant C/T snv 0.56 0.700 1.000 6 2015 2019
dbSNP: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.700 1.000 6 2007 2019
dbSNP: rs10920678
rs10920678
BRINP3
1 1 190270777 intron variant A/G snv 0.58 0.700 1.000 5 2015 2019
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: rs12454712
rs12454712
BCL2
9 0.925 0.120 18 63178651 intron variant T/A;C snv 0.700 1.000 5 2016 2019
dbSNP: rs17724992
rs17724992
PGPEP1
1 19 18344015 intron variant A/G snv 0.23 0.700 1.000 5 2015 2018
dbSNP: rs205262
rs205262
ILRUN
2 6 34595387 intron variant A/G snv 0.38 0.700 1.000 5 2015 2018
dbSNP: rs2075650
rs2075650
TOMM40
45 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 5 2015 2019
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: rs4740619
rs4740619
CCDC171
1 9 15634328 intron variant T/A;C snv 0.700 1.000 5 2015 2019