Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs549220260
CHAF1A
19 4426168 intron variant TTTTTTTT/-;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT delins 2
rs35676364
ILKAP
2 238184733 intron variant TTTTT/-;TTTT;TTTTTT;TTTTTTT;TTTTTTTT delins 2
rs11315539
RAB11A ; LOC105370866
15 65805720 intron variant TTTTT/-;T;TT;TTT;TTTT;TTTTTT;TTTTTTTT delins 0.69 1
rs66682515 3 196094159 intergenic variant TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTTTTTTTTTTTT delins 0.69 1
rs55649226
TFRC
3 196076452 intron variant TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTTTTTT delins 0.45 1
rs11301805
TNRC6B
22 40196077 intron variant TTT/-;T;TT;TTTT;TTTTTTTTT delins 0.68 1
rs33964027
EXOSC9
4 121808259 intron variant TTAC/- delins 0.31 2
rs560097346
ZKSCAN8
6 28149825 intron variant TT/-;T;TTT;TTTT delins 1
rs532398216 16 182398 downstream gene variant TGAG/- delins 2.0E-03 5
rs145364311
EPHX3
19 15232554 intron variant TC/-;TCTC delins 1
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
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
rs6904897
HBS1L
6 135061842 intron variant T/G snv 0.34 3
rs4820091
UBE2L3
22 21585900 intron variant T/G snv 0.30 2
rs78476878 19 33252092 regulatory region variant T/G snv 0.17 2
rs826415
TENT5C
1 117611355 intron variant T/G snv 0.27 2
rs11464707
TENT5C
1 117618398 intron variant T/G snv 0.18 1
rs2395792
USP49
6 41884449 intron variant T/G snv 0.97 1
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 7
rs429150
TNXB
1.000 6 32107786 intron variant T/C;G snv 6
rs62160676
MIR4435-2HG
2 111410354 intron variant T/C;G snv 5
rs932316 6 25640972 upstream gene variant T/C;G snv 4
rs496321
LOC101929295
11 95153468 intron variant T/C;G snv 3