Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs974404
AP4B1-AS1 ; PTPN22
1.000 0.080 1 113839403 intron variant G/A;T snv 1
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 1
rs174577
FADS2
1.000 0.080 11 61837342 intron variant C/A snv 0.38 1
rs718772
HORMAD2
0.925 0.120 22 30108218 intron variant A/C;G snv 1
rs2656069
IREB2
0.882 0.080 15 78453365 intron variant C/G;T snv 1
rs886424
LINC00243
0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 1
rs974494
LOC105372974 ; SEZ6L
1.000 0.080 22 26254399 intron variant C/G;T snv 1
rs75316749
LOC107986051
0.701 0.280 3 169043635 intergenic variant A/G snv 4.2E-02 1
rs116895242
LOC107986841
1.000 0.080 7 124306349 intron variant T/A snv 2.6E-02 1
rs3134942
NOTCH4
0.790 0.320 6 32200994 synonymous variant G/T snv 9.7E-02 0.11 1
rs968643096
RB1
1.000 0.080 13 48453041 missense variant C/T snv 1
rs34978822
RTEL1 ; RTEL1-TNFRSF6B
1.000 0.080 20 63660246 intron variant C/G snv 1.2E-02 1
rs13314271
TP63
0.925 0.080 3 189639813 intron variant T/C snv 0.45 1
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 1
rs2844573 0.882 0.160 6 31367677 intron variant A/C;G snv 2
rs4635969 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 2
rs680244
CHRNA5
0.882 0.120 15 78578946 intron variant T/C snv 0.60 2
rs174549
FADS2 ; FADS1
0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26 2
rs761896295
FGFR3
1.000 0.080 4 1804450 missense variant G/A snv 2.4E-05 2.1E-05 2
rs13180
IREB2
0.851 0.160 15 78497146 synonymous variant C/T snv 0.54 0.51 2
rs2734986
LOC105375010
0.827 0.160 6 29850791 intron variant T/C snv 0.10 2
rs12144215
MAGI3
0.925 0.120 1 113644533 intron variant G/A;T snv 2
rs10849605
RAD52
0.882 0.080 12 955272 intron variant T/C snv 0.49 2
rs863224682
TP53
1.000 0.080 17 7669655 missense variant C/A;T snv 4.0E-06 2
rs10508266 0.882 0.080 10 3797822 intergenic variant G/A;T snv 3