Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1906599 4 110791530 upstream gene variant T/C snv 0.67 1
rs1937787 1 80373593 non coding transcript exon variant T/C snv 0.23 1
rs1952706 14 36205321 intergenic variant C/G;T snv 1
rs1986743
ARL6IP6
2 152730385 intron variant A/G;T snv 1
rs202680
FOLH1
11 49200333 synonymous variant T/A snv 0.31 0.37 1
rs2084637
MIR100HG
11 122520479 intron variant T/C snv 0.27 1
rs2084898
TRIM29
11 120156040 intron variant G/A snv 9.3E-02 1
rs215976
CACNA1C
12 2585472 missense variant C/G;T snv 0.11 1
rs225132 1 8035440 intron variant T/G snv 0.27 1
rs2283436
ABHD2
15 89188545 intron variant T/C snv 9.6E-02 1
rs229961 5 57690889 regulatory region variant T/C snv 0.87 1
rs2304556
FMNL2
2 152617280 intron variant T/G snv 0.36 1
rs2415317
LINC00609 ; PTCSC3
14 36140472 intron variant G/A snv 0.46 1
rs243832
MMP2
16 55505279 intron variant C/G snv 0.50 1
rs248812 12 97667368 intergenic variant C/A snv 0.74 1
rs2632512
TSPOAP1-AS1 ; RNF43
17 58374461 intron variant T/C snv 0.85 1
rs2736122
TERT
5 1257506 intron variant G/A snv 0.23 1
rs2787417 14 36182597 intergenic variant T/C snv 0.66 1
rs2815063 6 39294759 downstream gene variant C/A snv 0.22 1
rs2822388
LOC105377134
21 14035713 intron variant A/G snv 4.9E-02 1
rs28688791
HDAC9
7 18999982 3 prime UTR variant T/A;C snv 1
rs28793911
ADAMTS13
9 133434817 intron variant T/C;G snv 1
rs3024718
PROZ
13 113159539 intron variant A/G snv 0.17 1
rs3024772
PCID2 ; PROZ
13 113171786 missense variant G/A;C snv 2.4E-02; 4.0E-06 1
rs3024778
PROZ
13 113160151 stop gained G/A;C;T snv 4.0E-06; 2.0E-05 1