Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2253612
AOX3P ; AOX3P-AOX2P
1.000 0.080 2 200703710 intron variant C/T snv 0.79 3
rs7590720
PECR ; MREG
1.000 0.080 2 216033935 intron variant G/A snv 0.73 3
rs72737330
ESRRG
0.925 0.080 1 216600151 intron variant T/C snv 0.15 4
rs6356
TH
0.827 0.240 11 2169721 missense variant C/T snv 0.43 0.32 1
rs10198241 0.925 0.080 2 226115660 intergenic variant T/C snv 0.58 4
rs7607774 1.000 0.080 2 236520511 intergenic variant G/A snv 7.4E-02 1
rs896543
LOC107986001
1.000 0.080 2 236600564 intergenic variant G/A snv 0.33 3
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 34
rs9512637 1.000 0.080 13 27346474 upstream gene variant T/C snv 0.55 3
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 64
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs2049045
BDNF-AS ; BDNF
1.000 0.080 11 27672694 intron variant G/A;C snv 0.13 2
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 3
rs29230
GABBR1
0.807 0.440 6 29608616 missense variant A/C;G snv 4.1E-06; 0.18 1
rs4478858
SERINC2
1.000 0.080 1 31411078 intron variant T/C snv 0.48 3
rs9378160
MICB
1.000 0.080 6 31500215 intron variant A/C;G snv 3
rs9282858
SRD5A2
0.716 0.320 2 31580756 missense variant C/T snv 1.8E-02 2.1E-02 7
rs2239803
HLA-DRA
0.882 0.240 6 32444056 intron variant C/A;T snv 0.50 3
rs4935356
HLA-DRA
1.000 0.080 6 32444611 intron variant T/A;G snv 1
rs6141509
NCOA6
1.000 0.080 20 34731584 intron variant G/A snv 0.45 3
rs6060038
NCOA6
1.000 0.080 20 34769912 intron variant G/A snv 0.45 3
rs6060124
GSS
1.000 0.080 20 34949094 intron variant C/A snv 0.27 1
rs3736802
TRPC4AP
1.000 0.080 20 35016239 intron variant T/C snv 0.53 3
rs4610908 1.000 0.080 X 35166418 intergenic variant G/A snv 0.24 1
rs11583322
STK40
1.000 0.080 1 36356711 intron variant T/C snv 0.30 1