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: rs1800629
rs1800629
TNF
169 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2009 2009
dbSNP: rs2562456
rs2562456
LINC00664
2 1.000 0.040 19 21483408 non coding transcript exon variant C/T snv 0.77 0.800 1.000 1 2009 2009
dbSNP: rs76060075
rs76060075
CYP2D6 ; NDUFA6-DT ; LOC112268294
2 1.000 0.120 22 42129185 missense variant C/G snv 0.010 1.000 1 2009 2009
dbSNP: rs8904
rs8904
NFKBIA
4 0.925 0.120 14 35402011 3 prime UTR variant G/A;C;T snv 0.39; 4.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs6265
rs6265
BDNF ; BDNF-AS
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.060 1.000 6 2010 2018
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
237 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 0.050 1.000 5 2010 2018
dbSNP: rs6746030
rs6746030
SCN9A ; SCN1A-AS1
16 0.763 0.320 2 166242648 missense variant A/G snv 0.88 0.88 0.040 1.000 4 2010 2018
dbSNP: rs165599
rs165599
ARVCF ; COMT
27 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 0.030 1.000 3 2010 2020
dbSNP: rs2032582
rs2032582
ABCB1
97 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.020 1.000 2 2010 2017
dbSNP: rs748653984
rs748653984
NTRK1
2 1.000 0.080 1 156868159 missense variant T/A;C snv 4.0E-06; 4.0E-06 0.020 1.000 2 2010 2011
dbSNP: rs778056858
rs778056858
NTRK1
2 1.000 0.080 1 156866944 missense variant T/C snv 8.0E-06 7.0E-06 0.020 1.000 2 2010 2011
dbSNP: rs1042713
rs1042713
ADRB2
63 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.010 1.000 1 2010 2010
dbSNP: rs12654778
rs12654778
ADRB2
1 5 148826178 5 prime UTR variant G/A snv 0.34 0.010 1.000 1 2010 2010
dbSNP: rs1378978590
rs1378978590
NGFR ; LOC100288866 ; MIR6165
1 17 49510504 stop gained C/T snv 0.010 1.000 1 2010 2010
dbSNP: rs200207721
rs200207721
OPRM1
2 6 154039743 missense variant A/G snv 1.2E-05 1.4E-05 0.010 1.000 1 2010 2010
dbSNP: rs28935468
rs28935468
MECP2
17 0.732 0.240 X 154030912 missense variant G/A snv 0.010 1.000 1 2010 2010
dbSNP: rs3813034
rs3813034
SLC6A4
8 0.827 0.160 17 30197786 3 prime UTR variant A/C snv 0.40 0.010 1.000 1 2010 2010
dbSNP: rs4778889
rs4778889
IL16
24 0.683 0.480 15 81296654 intron variant T/C snv 0.24 0.010 1.000 1 2010 2010
dbSNP: rs61748421
rs61748421
MECP2
9 0.807 0.200 X 154031326 stop gained G/A;T snv 0.010 1.000 1 2010 2010
dbSNP: rs61751364
rs61751364
MECP2
4 0.882 0.120 X 154030944 frameshift variant CGGAT/- delins 0.010 1.000 1 2010 2010
dbSNP: rs769540300
rs769540300
OPRM1
8 0.851 0.200 6 154091047 missense variant G/A snv 1.2E-05 0.010 1.000 1 2010 2010
dbSNP: rs769854785
rs769854785
NTRK1
1 1 156871656 synonymous variant C/T snv 0.010 1.000 1 2010 2010
dbSNP: rs77114424
rs77114424
OPRM1
2 6 154039497 missense variant G/A snv 0.010 1.000 1 2010 2010
dbSNP: rs893924483
rs893924483
BDNF ; BDNF-AS
23 0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 0.010 1.000 1 2010 2010
dbSNP: rs941601
rs941601
SERPINA6
1 14 94305204 intron variant C/T snv 0.19 0.010 1.000 1 2010 2010