Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs371642320
LUC7L
16 193807 intron variant TTTT/-;TT;TTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTTTTTTT delins 1
rs374588807
UBE2L3
22 21584179 intron variant TTT/-;T;TT;TTTT;TTTTT delins 0.21 1
rs532398216 16 182398 downstream gene variant TGAG/- delins 2.0E-03 5
rs57583458
FAM222B
17 28779752 intron variant TAAATAAATAAATAAATAAATAAATAAA/-;TAAATAAATAAA;TAAATAAATAAATAAA;TAAATAAATAAATAAATAAA;TAAATAAATAAATAAATAAATAAA;TAAATAAATAAATAAATAAATAAATAAATAAA;TAAATAAATAAATAAATAAATAAATAAATAAATAAA;TAAATAAATAAATAAATAAATAAATAAATAAATAAATAAA delins 1
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs7203560
NPRL3
1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 7
rs632057 6 139512875 intron variant T/G snv 0.57 5
rs1408272
SLC17A3
6 25842723 intron variant T/G snv 4.0E-02 4
rs1997672
CARMIL1
0.925 0.120 6 25617316 intron variant T/G snv 0.28 4
rs2074404
LRRC37A2 ; WNT3
0.925 0.120 17 46788073 intron variant T/G snv 0.27 4
rs4082919
PGS1
17 78381401 intron variant T/G snv 0.55 4
rs9295681 0.925 0.120 6 25943889 intergenic variant T/G snv 0.37 4
rs9393672
SLC17A3
0.925 0.120 6 25842377 intron variant T/G snv 0.51 4
rs12669559
IKZF1
1.000 0.120 7 50368079 synonymous variant T/G snv 0.35 0.32 3
rs1892253
SLC17A1
0.925 0.120 6 25782086 downstream gene variant T/G snv 0.86 3
rs4409177
SCGN
0.925 0.120 6 25694263 intron variant T/G snv 0.25 3
rs6904897
HBS1L
6 135061842 intron variant T/G snv 0.34 3
rs10484435
H3C2
1.000 0.040 6 26031583 upstream gene variant T/G snv 7.6E-02 2
rs11753329
USP49
6 41820642 intron variant T/G snv 0.14 2
rs11754384 1.000 0.040 6 26322757 upstream gene variant T/G snv 0.13 2
rs12435835
MAX ; CHURC1-FNTB ; FNTB
14 65033191 intron variant T/G snv 0.57 2
rs149489081
ANK1
8 41732218 intron variant T/G snv 5.8E-03 2
rs17572495
MAPT
1.000 0.080 17 45977230 non coding transcript exon variant T/G snv 0.14 2
rs17763086
MAPT-AS1 ; CRHR1 ; LINC02210-CRHR1
1.000 0.040 17 45828115 intron variant T/G snv 0.14 2
rs199534
NSF ; LRRC37A2
1.000 0.120 17 46746847 intron variant T/G snv 0.13 2