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: rs11178999
rs11178999
TPH2
1 12 71939790 intron variant G/A snv 0.27 0.010 1.000 1 2019 2019
dbSNP: rs11624704
rs11624704
NRXN3
3 1.000 0.080 14 78319734 intron variant A/C snv 0.13 0.010 1.000 1 2011 2011
dbSNP: rs11819869
rs11819869
AMBRA1
2 1.000 0.040 11 46539130 intron variant C/T snv 0.27 0.010 1.000 1 2013 2013
dbSNP: rs12765063
rs12765063
CREM ; CUL2
2 10 35127641 intron variant G/A snv 0.14 0.010 1.000 1 2018 2018
dbSNP: rs1360780
rs1360780
FKBP5 ; LOC112267956
31 0.708 0.320 6 35639794 intron variant T/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs1386483
rs1386483
TPH2
9 0.790 0.080 12 72018714 intron variant T/C snv 0.53 0.010 1.000 1 2009 2009
dbSNP: rs1455858
rs1455858
CHRM2 ; LOC349160
3 0.925 0.080 7 136946956 intron variant T/C snv 0.69 0.010 1.000 1 2011 2011
dbSNP: rs1473473
rs1473473
TPH2
4 0.925 0.080 12 72010598 intron variant C/A;T snv 0.81 0.010 1.000 1 2013 2013
dbSNP: rs1535255
rs1535255
CNR1
8 0.807 0.120 6 88151489 intron variant T/G snv 0.21 0.010 1.000 1 2007 2007
dbSNP: rs2023239
rs2023239
CNR1
20 0.724 0.160 6 88150763 intron variant T/C snv 0.21 0.010 1.000 1 2007 2007
dbSNP: rs2030324
rs2030324
BDNF
6 0.827 0.120 11 27705368 intron variant A/G snv 0.49 0.010 1.000 1 2015 2015
dbSNP: rs2044081
rs2044081
GABRB1
2 1.000 0.080 4 47216323 intron variant C/T snv 0.14 0.010 1.000 1 2017 2017
dbSNP: rs2161961
rs2161961
GNAL
3 18 11774501 intron variant A/G snv 0.31 0.010 1.000 1 2008 2008
dbSNP: rs2261722
rs2261722
PCSK5
1 9 76254665 intron variant G/A snv 0.30 0.010 1.000 1 2012 2012
dbSNP: rs2284411
rs2284411
GRIN2B
4 1.000 0.040 12 13713238 intron variant C/T snv 0.34 0.010 1.000 1 2017 2017
dbSNP: rs402691
rs402691
PRKCG
2 19 53888383 intron variant T/C snv 0.39 0.010 1.000 1 2007 2007
dbSNP: rs4659682
rs4659682
LGALS8
1 1 236518948 intron variant A/G snv 0.62 0.010 1.000 1 2012 2012
dbSNP: rs478597
rs478597
NOS1
2 1.000 0.040 12 117313620 intron variant G/A snv 0.35 0.010 1.000 1 2016 2016
dbSNP: rs591556
rs591556
TPH1
1 11 18039853 intron variant T/C snv 0.78 0.010 1.000 1 2019 2019
dbSNP: rs594242
rs594242
HTR2A
3 1.000 0.040 13 46883917 intron variant C/A;G snv 0.010 1.000 1 2006 2006
dbSNP: rs806379
rs806379
CNR1
2 1.000 0.040 6 88151548 intron variant A/C;T snv 0.010 1.000 1 2015 2015
dbSNP: rs11617488
rs11617488
LOC107984582
1 13 21619823 intergenic variant A/G snv 0.27 0.010 1.000 1 2012 2012
dbSNP: rs2110267
rs2110267
DPP6
3 1.000 0.040 7 153838604 intergenic variant C/G snv 0.32 0.010 1.000 1 2013 2013
dbSNP: rs79874540
rs79874540
HTR2B ; PSMD1
4 0.925 0.080 2 231123707 stop gained G/A snv 1.5E-03 1.2E-03 0.020 1.000 2 2015 2017
dbSNP: rs886041097
rs886041097
NAA15
9 0.882 0.160 4 139386152 stop gained C/G snv 0.700 0