Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16841143
PTH2R
2 208384849 intron variant G/A snv 0.13 2
rs182087934 2 183742707 intergenic variant G/A snv 2
rs384005
MEF2C-AS2
5 88709286 intron variant T/C snv 0.70 2
rs4554696
PDE4B
1 65942328 intron variant C/T snv 0.33 2
rs62199592 2 183858773 intergenic variant A/G snv 2.1E-02 2
rs6475417
SLC24A2
9 20212043 intergenic variant A/G;T snv 2
rs6661750
PDE4B
1 66081201 intron variant A/G;T snv 2
rs11123857
NPAS2
2 100987350 non coding transcript exon variant A/G snv 0.29 1
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 6
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 1
rs4625
DAG1
0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs659366
UCP2
0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 1
rs2251219
SMIM4 ; PBRM1
0.732 0.120 3 52550771 synonymous variant T/C;G snv 0.39; 4.0E-06 0.34 3
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 2
rs11039149
NR1H3
0.827 0.280 11 47255124 intron variant A/G snv 0.19 2
rs7597593
ZNF804A
0.827 0.160 2 184668853 intron variant T/C snv 0.53 2
rs2522833
PCLO
0.827 0.080 7 82824392 missense variant A/C snv 0.45 0.34 1
rs841
GCH1
0.827 0.200 14 54843774 splice region variant G/A snv 0.22 0.22 1
rs12938031
LINC02210-CRHR1
0.851 0.160 17 45777136 intron variant A/G snv 0.26 4
rs8007267 0.882 0.200 14 54912273 intergenic variant C/T snv 0.31 1
rs7225002
KANSL1
0.925 0.080 17 46111701 intron variant A/G snv 0.39 7