Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11677607
AFF3
2 100134688 intron variant C/T snv 0.24 1
rs73966422
AFF3
2 100137627 non coding transcript exon variant C/G;T snv 1
rs72755233
ADAMTS17
1.000 0.080 15 100152748 missense variant G/A;T snv 7.1E-02; 3.2E-05 5
rs400301
CIDECP1
3 10015782 intron variant G/A snv 6.8E-02 1
rs57989773 1.000 0.080 6 100181202 downstream gene variant T/C snv 0.23 2
rs13002946
AFF3
2 100185497 intron variant T/A snv 0.25 1
rs6542924
LONRF2
2 100276651 3 prime UTR variant C/A;G snv 1
rs4851287
LONRF2
2 100299310 missense variant A/G snv 0.69 0.72 1
rs9299338
TEX10
9 100345896 intron variant A/G;T snv 1
rs17094222 0.925 0.080 10 100635683 intergenic variant T/C snv 0.17 3
rs2495707 10 100666192 downstream gene variant A/G snv 0.21 1
rs12147845 14 100678259 intron variant C/T snv 0.10 1
rs180963
ASCC3
6 100679337 intron variant T/C snv 0.52 1
rs41310284 10 100687890 intergenic variant C/A;T snv 3
rs6907240
ASCC3
6 100705906 intron variant T/C;G snv 1
rs12209887
ASCC3
6 100708930 intron variant G/A snv 0.47 1
rs34277166 10 100875096 regulatory region variant G/A snv 0.40 1
rs1799805
ACHE
7 100893176 missense variant G/T snv 4.0E-02 3.2E-02 1
rs10883560
SLF2
10 100913950 intron variant C/G;T snv 1
rs3134353
YWHAZ
8 100935225 intron variant A/C;G;T snv 1
rs3134358
YWHAZ
8 100946205 intron variant G/T snv 0.66 1
rs7817485 8 100957300 upstream gene variant T/C;G snv 0.66 1
rs7161194
MIR541
14 101062668 upstream gene variant A/G;T snv 2
rs7147503
LOC105370670 ; MEG9
14 101073047 intron variant C/T snv 0.32 1
rs12431682
LOC105370670
14 101073662 intron variant C/T snv 0.32 1