Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs59314616
LOC105369944
12 102561501 intergenic variant TTTTTTTT/-;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT delins 1
rs11380688
HCG17 ; HCG18
6 30305977 non coding transcript exon variant TTTT/-;TTT;TTTTT;TTTTTT;TTTTTTTTT delins 1
rs71555635
PLAG1
8 56201961 intron variant TTTT/-;TT;TTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT delins 1
rs72556249
SENP6
6 75653661 intron variant TT/-;T;TTT;TTTT delins 2.0E-02 1
rs34710064
LCORL
4 17963642 intron variant TT/-;T;TTT delins 1
rs139901282
ID4
6 19840722 3 prime UTR variant TT/- del 0.28 1
rs200235318
ZBTB38
3 141394029 intron variant TG/- del 1
rs2004640
IRF5
0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
rs45446698
CYP3A7-CYP3A51P ; CYP3A7 ; ZSCAN25
0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02 9
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 6
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs7753012
ADGRG6
6 142424746 intron variant T/G snv 0.50 5
rs2280141
PLEKHA1
1.000 0.040 10 122433665 3 prime UTR variant T/G snv 0.56 4
rs473902
PTCH1
9 95493953 intron variant T/G snv 5.7E-02 4
rs6918725
LOC105377992
6 126669246 intron variant T/G snv 0.50 4
rs6894139
MEF2C-AS1
5 89031965 non coding transcript exon variant T/G snv 0.57 3
rs6937121
ADGRG6
6 142385996 intron variant T/G snv 0.47 3
rs7183263
ADAMTSL3
15 83904289 intron variant T/G snv 0.63 3
rs946053
COL27A1
1.000 9 114287611 intron variant T/G snv 0.63 3
rs10818576
DAB2IP
1.000 0.040 9 121650669 intron variant T/G snv 0.21 2
rs10838798
PTPRJ
11 48069751 intron variant T/G snv 0.56 2
rs1150668
ZNF192P1
6 28162011 intron variant T/G snv 0.58 2
rs12470505
CFAP65
2 219043647 upstream gene variant T/G snv 0.19 2
rs153750 5 171754233 intergenic variant T/G snv 0.71 2