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: rs1805054
rs1805054
HTR6
17 0.708 0.200 1 19666020 synonymous variant C/T snv 0.15; 8.0E-06 0.16 0.010 1.000 1 2001 2001
dbSNP: rs1800041
rs1800041
HTR1A
4 0.882 0.120 5 63961673 missense variant G/A snv 1.8E-03 5.3E-04 0.010 1.000 1 2004 2004
dbSNP: rs74315401
rs74315401
PRNP
32 0.683 0.320 20 4699525 missense variant C/T snv 0.010 1.000 1 2004 2004
dbSNP: rs63750424
rs63750424
MAPT
30 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.010 1.000 1 2005 2005
dbSNP: rs1800035
rs1800035
ADRA2A
4 0.925 0.080 10 111078794 missense variant C/G;T snv 1.9E-03 0.010 < 0.001 1 2006 2006
dbSNP: rs4713916
rs4713916
FKBP5
11 0.790 0.160 6 35702206 intron variant A/C;G;T snv 0.010 1.000 1 2006 2006
dbSNP: rs553040076
rs553040076
PDE4A ; CDC37
3 0.925 0.080 19 10417700 missense variant T/A snv 4.5E-05 7.7E-05 0.010 1.000 1 2007 2007
dbSNP: rs747052707
rs747052707
FOLH1
3 0.925 0.080 11 49192822 missense variant T/C snv 2.4E-05; 8.1E-06 0.010 1.000 1 2007 2007
dbSNP: rs1013940
rs1013940
SLC5A7
6 0.827 0.160 2 107992192 missense variant A/G snv 9.3E-02 7.4E-02 0.010 1.000 1 2008 2008
dbSNP: rs1176744
rs1176744
HTR3B
19 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 0.010 1.000 1 2008 2008
dbSNP: rs1805087
rs1805087
MTR
135 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2008 2008
dbSNP: rs2242446
rs2242446
SLC6A2
9 0.776 0.080 16 55656513 5 prime UTR variant C/A;T snv 0.010 1.000 1 2008 2008
dbSNP: rs28386840
rs28386840 		6 0.827 0.080 16 55652906 upstream gene variant T/A;C snv 0.010 1.000 1 2008 2008
dbSNP: rs36010656
rs36010656
SLCO1C1
4 0.925 0.080 12 20711408 missense variant C/A;T snv 3.4E-02 0.010 1.000 1 2008 2008
dbSNP: rs749437638
rs749437638
ARVCF ; COMT
14 0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05 0.010 1.000 1 2008 2008
dbSNP: rs1220000453
rs1220000453
CNTF ; ZFP91-CNTF
5 0.882 0.120 11 58624189 synonymous variant C/T snv 0.020 1.000 2 2006 2009
dbSNP: rs662
rs662
PON1
157 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.020 1.000 2 2007 2009
dbSNP: rs1187329
rs1187329
NTRK2
3 0.925 0.080 9 84674365 intron variant A/G snv 0.52 0.010 1.000 1 2009 2009
dbSNP: rs11911834
rs11911834
S100B
4 0.882 0.080 21 46602608 5 prime UTR variant G/A;T snv 0.010 1.000 1 2009 2009
dbSNP: rs1232898090
rs1232898090
PPARA
40 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs12936511
rs12936511
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
5 0.925 0.080 17 45807036 synonymous variant C/T snv 3.1E-02 3.0E-02 0.010 1.000 1 2009 2009
dbSNP: rs1800044
rs1800044
HTR1A
8 0.827 0.200 5 63961061 missense variant C/A snv 3.7E-03 3.8E-03 0.010 1.000 1 2009 2009
dbSNP: rs1801282
rs1801282
PPARG
131 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2009 2009
dbSNP: rs1805192
rs1805192
PPARG
121 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2009 2009
dbSNP: rs2020936
rs2020936
SLC6A4
10 0.776 0.160 17 30223796 intron variant G/A;C snv 0.010 1.000 1 2009 2009