Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1271572
ESR2
0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs1020397
ARNT2
0.882 0.160 15 80426396 intron variant G/C;T snv 3
rs2278705 0.882 0.160 15 80402288 intron variant C/T snv 4.2E-02 3
rs2472680
NR1I2
0.882 0.160 3 119808929 intron variant T/C snv 0.90 3
rs5000770
ARNT2
0.882 0.160 15 80424141 intron variant G/A snv 0.27 3
rs6932902
ESR1
0.882 0.160 6 152055389 intron variant G/A snv 0.22 3
rs11091748
DGKK
0.925 0.120 X 50414986 intron variant A/G snv 0.39 2
rs12171755
DGKK
0.925 0.120 X 50436751 intron variant C/T snv 0.30 2
rs1256062
ESR2
0.925 0.120 14 64236600 intron variant T/C snv 0.21 2
rs1858800
ZFHX3
1.000 0.120 16 72990377 intron variant C/T snv 0.28 2
rs1934179
DGKK
0.925 0.120 X 50439186 intron variant G/A snv 0.46 2
rs1934190
DGKK
0.925 0.120 X 50400967 intron variant G/A;C snv 0.33 2
rs2211122
DGKK
0.925 0.120 X 50459752 intron variant T/C snv 0.45 2
rs4554617
DGKK
0.925 0.120 X 50460404 intron variant A/C snv 0.45 2
rs4599945
DGKK
0.925 0.120 X 50380968 intron variant G/A;T snv 2
rs4826632
DGKK
0.925 0.120 X 50454263 intron variant G/T snv 0.46 2
rs6499755 0.925 0.120 16 55307223 intron variant T/C snv 0.30 2
rs10214930
TAX1BP1
1.000 0.120 7 27745330 intron variant G/A snv 0.20 1
rs10762738
KCNMA1 ; KCNMA1-AS1
1.000 0.120 10 76935709 intron variant A/G snv 0.38 1
rs10979
PHACTR2 ; PHACTR2-AS1
1.000 0.120 6 143568902 intron variant G/A snv 0.62 1
rs16937456
LOC105375894
1.000 0.120 8 71165720 intron variant A/G;T snv 1
rs17262815
CCDC26
1.000 0.120 8 129478919 intron variant T/C snv 0.13 1
rs17747401
ADK
1.000 0.120 10 74640406 intron variant C/T snv 0.27 1
rs1918690
DNAH6
1.000 0.120 2 84679791 intron variant T/C snv 0.74 1
rs2999052
EEFSEC
1.000 0.120 3 128173194 intron variant T/C snv 0.30 1