Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8067056
MAPT
0.925 0.080 17 46006582 intron variant T/C;G snv 0.30 5
rs9303521
LINC02210-CRHR1
0.925 0.120 17 45727828 intron variant T/C;G snv 0.60 5
rs199505
WNT3 ; LRRC37A2
0.925 0.120 17 46782044 intron variant A/G snv 0.84 4
rs62081501 0.925 0.080 18 37627749 intron variant G/A snv 6.2E-02 4
rs111365677 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 3
rs112106319
TNC ; DELEC1
0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03 3
rs112538845 0.925 0.040 4 184084475 downstream gene variant C/T snv 1.7E-02 3
rs11924809
DGKG
0.925 0.040 3 186353656 intron variant G/A snv 5.3E-02 3
rs142484554
SPSB4
0.925 0.040 3 141059454 intron variant GAG/- delins 0.11 3
rs142641502
CSTF3
0.925 0.040 11 33109861 intron variant T/C snv 8.0E-03 3
rs143405544
ADAMTS6
0.925 0.040 5 65459777 intron variant A/G snv 4.8E-03 3
rs143934587 0.925 0.040 20 19165806 intergenic variant G/A snv 9.1E-03 3
rs1548076 0.925 0.040 15 69934284 intergenic variant G/A snv 0.95 3
rs182377406 0.925 0.040 11 67449378 upstream gene variant A/G snv 4.5E-04 3
rs183042538
ZHX3
0.925 0.040 20 41197420 intron variant A/T snv 3.2E-02 3
rs183124483
NLK
0.925 0.040 17 28110028 intron variant G/A snv 7.1E-04 3
rs188843168
ATP5MD
0.925 0.040 10 103390184 intron variant T/A;C snv 4.3E-04 3
rs189864513
LINC01618
0.925 0.040 4 52767390 intron variant T/C snv 1.9E-03 3
rs190783615 0.925 0.040 X 142772620 intergenic variant T/C snv 9.3E-03 3
rs1908557 0.925 0.040 4 89500202 intron variant T/C snv 0.31 3
rs200855945
SSPN ; BHLHE41
0.925 0.040 12 26124961 5 prime UTR variant ACACGCACAC/-;ACACGCACACACACGCACAC delins 1.6E-02 3
rs201203751
FYB1
0.925 0.040 5 39203496 intron variant TT/-;T;TTT delins 3
rs201569130 0.925 0.040 6 1402916 intergenic variant GACA/- delins 1.1E-02 3
rs201921722 0.925 0.040 11 123679999 downstream gene variant -/A delins 9.2E-06 3
rs2435200
MAPT
0.925 0.080 17 45994485 intron variant G/A snv 0.40 3