Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs73788091
FSTL4 ; MIR1289-2
1.000 0.040 5 133429517 intron variant C/T snv 0.10 3
rs7613360 1.000 0.040 3 49879277 upstream gene variant C/T snv 0.32 3
rs7939345 1.000 0.040 11 47959016 intergenic variant T/A;G snv 3
rs80164876
LOC105374732 ; EGFLAM
1.000 0.040 5 38464142 3 prime UTR variant A/G snv 1.9E-02 3
rs8100891 1.000 0.040 19 32338607 intergenic variant C/A;G snv 3
rs10020288 1.000 0.040 4 28686220 intergenic variant G/A snv 0.38 2
rs10144845
YLPM1
1.000 0.040 14 74771067 intron variant C/T snv 0.62 2
rs10156548 1.000 0.040 9 23318435 intron variant G/C;T snv 2
rs10405382
DPY19L3 ; LOC400684
1.000 0.040 19 32405810 5 prime UTR variant C/G snv 0.18 2
rs10429537 1.000 0.040 9 23346844 intron variant C/G snv 0.33 2
rs1055447
ARFGAP2 ; C11orf49
1.000 0.040 11 47164873 3 prime UTR variant C/A;T snv 2
rs10891564 1.000 0.040 11 113503291 intergenic variant G/A snv 0.34 2
rs10950393
TMEM106B
1.000 0.040 7 12223920 intron variant T/C snv 0.50 2
rs11039409
NUP160
1.000 0.040 11 47814169 intron variant A/C snv 0.22 2
rs11152363
TCF4
1.000 0.040 18 55389957 intron variant G/A snv 0.16 2
rs11209175
GNG12-AS1
1.000 0.040 1 67909145 intron variant C/T snv 0.54 2
rs11214589
TTC12
1.000 0.040 11 113374326 intron variant G/A snv 0.36 2
rs11214607
DRD2
1.000 0.040 11 113441417 intron variant T/G snv 0.16 2
rs11514731
MAD1L1
1.000 0.040 7 2011868 intron variant C/G snv 0.16 2
rs11599236
SORCS3
1.000 0.040 10 104694914 intron variant T/C;G snv 2
rs11605020
LOC105369562
1.000 0.040 11 127110970 intron variant G/A;C snv 2
rs11608355
MYO1H
1.000 0.040 12 109441487 intron variant T/C snv 0.33 2
rs116362708
SLC44A5
1.000 0.040 1 75464629 intron variant G/A snv 2.3E-02 2
rs11663393
DCC
1.000 0.040 18 53088362 intron variant G/A snv 0.40 2
rs11664123
DCC
1.000 0.040 18 53440658 intron variant T/C snv 0.24 2