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: rs41423247
rs41423247
NR3C1
23 0.695 0.440 5 143399010 intron variant G/C snv 0.31 0.010 1.000 1 2019 2019
dbSNP: rs4290270
rs4290270
TPH2
17 0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 0.010 1.000 1 2012 2012
dbSNP: rs4680
rs4680
COMT ; MIR4761
249 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 0.010 1.000 1 2008 2008
dbSNP: rs4795541
rs4795541
SLC6A4 ; LOC105371720
7 0.807 0.200 17 30237299 upstream gene variant A/G snv 0.010 1.000 1 2012 2012
dbSNP: rs5374
rs5374
GALR1
1 1.000 0.080 18 77250689 synonymous variant T/C snv 0.57 0.57 0.010 1.000 1 2014 2014
dbSNP: rs6561333
rs6561333
HTR2A
1 1.000 0.080 13 46846177 intron variant T/C snv 0.60 0.010 1.000 1 2013 2013
dbSNP: rs6713532
rs6713532
POMC
1 1.000 0.080 2 25161964 intron variant T/C snv 0.36 0.010 1.000 1 2009 2009
dbSNP: rs6719226
rs6719226 		1 1.000 0.080 2 25173143 upstream gene variant C/G snv 0.13 0.010 1.000 1 2009 2009
dbSNP: rs678849
rs678849
OPRD1
5 0.882 0.120 1 28818676 intron variant C/T snv 0.44 0.010 1.000 1 2013 2013
dbSNP: rs684513
rs684513
CHRNA5
5 0.925 0.080 15 78566058 intron variant C/G;T snv 0.010 1.000 1 2010 2010
dbSNP: rs6871510
rs6871510
HOMER1
1 1.000 0.080 5 79496521 intron variant C/T snv 0.22 0.010 1.000 1 2005 2005
dbSNP: rs6989250
rs6989250 		1 1.000 0.080 8 53253835 upstream gene variant C/G;T snv 0.010 1.000 1 2013 2013
dbSNP: rs779838446
rs779838446
CHRNA6
2 0.925 0.080 8 42756217 missense variant G/A snv 4.0E-06 7.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs806368
rs806368
CNR1
14 0.752 0.280 6 88140381 3 prime UTR variant T/C snv 0.19 0.010 1.000 1 2009 2009