Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28363170
SLC6A3
0.827 0.120 5 1393745 3 prime UTR variant -/AGTGGGGGCCCTGCATGCGTCCTGGGGTAGTACACGCTCC delins 8.1E-06 7
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs11568822
APOC1
1.000 0.080 19 44914381 5 prime UTR variant -/CGTT delins 1
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs1455460144
CHAT
1.000 0.080 10 49625580 frameshift variant A/- del 7.0E-06 1
rs4646
MIR4713HG ; CYP19A1
0.716 0.360 15 51210647 3 prime UTR variant A/C snv 0.67 0.70 16
rs242941
MAPT-AS1 ; CRHR1 ; LINC02210-CRHR1
0.790 0.200 17 45815154 intron variant A/C snv 0.62 9
rs63750311
PSEN1
0.790 0.240 14 73192647 missense variant A/C snv 7
rs1362575880
PSEN1
0.851 0.120 14 73192840 missense variant A/C snv 4.0E-06 4
rs1133763
CCL8
0.882 0.200 17 34320812 missense variant A/C snv 0.21 0.15 3
rs63749964
APP
0.851 0.080 21 25891783 missense variant A/C snv 3
rs7840202
UBR5
0.851 0.160 8 102296172 intron variant A/C snv 0.21 3
rs1036819
ZFAT-AS1 ; ZFAT
0.925 0.120 8 134599702 non coding transcript exon variant A/C snv 0.11 2
rs1200601649
APP
0.925 0.080 21 26022022 missense variant A/C snv 2
rs157590
TOMM40
0.882 0.160 19 44895459 intron variant A/C snv 0.60 2
rs201093867
APP
0.925 0.080 21 26021995 missense variant A/C snv 2
rs63750888
PSEN1
0.925 0.080 14 73192828 missense variant A/C snv 2
rs730437
EGFR
0.925 0.120 7 55147325 intron variant A/C snv 0.51 2
rs10997691
CTNNA3
1.000 0.080 10 67521827 intron variant A/C snv 0.16 0.13 1
rs1167428194
APOE
1.000 0.080 19 44908634 missense variant A/C snv 1
rs121908402
TREM2 ; LOC105375056
0.882 0.280 6 41161277 missense variant A/C snv 1.2E-05 1
rs1408585874
CAMK1 ; OGG1
1.000 0.080 3 9757233 missense variant A/C snv 4.0E-06 1
rs2274705
ESR2
1.000 0.080 14 64249911 intron variant A/C snv 0.18 1
rs2965169
BCL3
0.925 0.120 19 44747899 non coding transcript exon variant A/C snv 0.50 1
rs4844610
CR1
1.000 0.080 1 207629207 intron variant A/C snv 0.87 1