Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1408579
ERLIN1
1.000 0.040 10 100152437 intron variant C/T snv 0.32 3
rs7157599
DEGS2
0.925 0.040 14 100159565 missense variant C/T snv 0.73 0.76 3
rs6712515
AFF3
0.925 0.160 2 100190052 intron variant T/A;C snv 3
rs117304774
GRIN2A
1.000 0.040 16 10057377 intron variant G/A snv 8.2E-03 2
rs221798
GIGYF1
0.882 0.040 7 100689872 intron variant C/A;G snv 3
rs221780 1.000 0.040 7 100699412 regulatory region variant G/C;T snv 2
rs221774 0.851 0.080 7 100701361 upstream gene variant A/G;T snv 4
rs506597 0.882 0.040 7 100715797 upstream gene variant A/G snv 0.90 4
rs1734907 0.925 0.080 7 100717894 upstream gene variant A/G snv 0.84 2
rs7214058
GAS7
1.000 0.040 17 10080017 intron variant T/A;G snv 2
rs644939
ANO4
1.000 0.040 12 101060211 intron variant G/A snv 0.24 1
rs13096071 1.000 0.040 3 101082799 intergenic variant T/A;C snv 1
rs114540395 1.000 0.040 10 101719305 intron variant C/T snv 9.2E-02 1
rs73191547
MSRA
1.000 0.040 8 10175915 intron variant A/T snv 0.28 2
rs6855246 1.000 0.040 4 102191313 intergenic variant A/G snv 0.14 4
rs35225200 1.000 0.040 4 102225731 intergenic variant A/C snv 5.4E-02 5
rs35518360 1.000 0.040 4 102225733 intergenic variant A/G;T snv 1
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 30
rs1035130
IL18R1
1.000 0.040 2 102384942 synonymous variant C/T snv 0.26 0.24 1
rs6878284
SLCO6A1
0.925 0.040 5 102434022 intron variant C/T snv 0.64 1
rs150634721
LOC105369944
1.000 0.040 12 102492363 intergenic variant C/G;T snv 1
rs1502844 1.000 0.040 5 102523613 regulatory region variant C/T snv 0.66 1
rs9665626
SUFU
1.000 0.040 10 102540881 intron variant C/G;T snv 1
rs7907645 1.000 0.040 10 102664043 downstream gene variant T/G snv 0.13 2
rs10883765
ARL3
1.000 0.040 10 102696929 intron variant T/C snv 0.11 1