Disease: Borderline Personality Disorder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2709370 0.851 0.120 2 207517878 intron variant A/C snv 0.17 4
rs6746896 0.851 0.120 2 96745212 intergenic variant A/G snv 0.26 4
rs778293 0.807 0.120 13 105516850 intergenic variant C/A;T snv 7
rs78089757 0.882 0.120 10 125424260 intergenic variant G/A snv 9.9E-03 3
rs1610037
ADCYAP1
0.925 0.120 18 910634 3 prime UTR variant A/G snv 0.26 2
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs746682028
BDNF ; BDNF-AS
0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs2284017
CACNG2
0.925 0.120 22 36700882 intron variant T/C snv 0.44 2
rs2284018
CACNG2
0.925 0.120 22 36701519 intron variant C/G;T snv 2
rs9836592
CHDH
0.925 0.120 3 53821056 intron variant C/T snv 0.74 2
rs6785
CREB1 ; METTL21A
0.851 0.120 2 207603273 3 prime UTR variant A/G snv 0.84 4
rs1938516
ERVMER61-1
0.925 0.120 1 187433789 intron variant T/A snv 5.7E-02 2
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs11199993
FGFR2
0.925 0.120 10 121531750 intron variant G/C snv 4.8E-02 2
rs187269
GABRB2
0.827 0.160 5 161329618 3 prime UTR variant A/G snv 0.34 6
rs2546620
GABRB2
0.882 0.120 5 161332120 intron variant T/C snv 0.15 3
rs7975
GSTZ1
0.763 0.320 14 77326864 stop gained G/A;C;T snv 0.31 0.32 9
rs1128306
HCG9 ; HLA-A
0.925 0.120 6 29975492 non coding transcript exon variant G/A snv 0.22 2
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs3786285
IMPA2
0.925 0.120 18 12008848 intron variant A/C;G snv 2
rs613993
IMPA2
0.925 0.120 18 12028581 non coding transcript exon variant A/G snv 0.33 2