Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2423279 0.790 0.080 20 7831703 downstream gene variant T/C snv 0.29 1
rs7717457 5 40887679 intergenic variant A/G snv 0.23 1
rs776225963
ATP4A
19 35555490 missense variant G/A;T snv 1.1E-04 1
rs1051992
CAVIN3 ; LOC101927825
11 6319476 missense variant A/G snv 4.2E-06; 0.55 0.51 1
rs11646171
CDH8
16 61824185 intron variant G/A snv 0.13 1
rs776968306
FGFR1OP
6 167024793 missense variant C/T snv 4.0E-06 1
rs2237306
GSDME
7 24717583 intron variant C/A;G;T snv 1
rs201894482
HSPA9
5 138557977 missense variant G/A snv 6.0E-05 2.1E-05 1
rs1261963959
KIF1B
1 10297069 missense variant G/A snv 4.0E-06 1
rs148526538
KRT5
12 52520269 missense variant G/A;C snv 8.9E-05; 4.0E-06 1
rs1634507
LOC101927369
17 36098180 regulatory region variant G/A;T snv 1
rs769394388
LOC105372629 ; HNF4A
20 44355829 missense variant G/A;T snv 1
rs587776946
LRIG2
1.000 1 113114471 stop gained C/T snv 1
rs72478580
PRLR
1.000 5 35072610 missense variant T/G snv 1.9E-02 1.9E-02 1
rs169724
SYK
9 90828217 intron variant T/C;G snv 1
rs182361
SYK
9 90828077 intron variant C/A snv 0.11 1
rs771939956
TP53
17 7670705 missense variant C/T snv 4.0E-06 7.0E-06 1
rs1453340173
TSHZ1
18 75286531 missense variant C/T snv 4.0E-06 1
rs1372834410
VGLL4 ; ATG7
3 11558705 missense variant C/T snv 1
rs17227424
ZNF276 ; FANCA
16 89738216 missense variant G/A;C snv 1.3E-05; 3.6E-02 1
rs29232 0.925 0.240 6 29643654 intergenic variant C/T snv 0.39 2
rs137854573
APC
0.807 0.120 5 112828889 stop gained C/T snv 2
rs137854574
APC
0.925 0.120 5 112828919 stop gained C/T snv 2
rs397509039
BRCA1
1.000 0.200 17 43092379 missense variant G/A;C snv 2
rs62625307
BRCA1
0.827 0.200 17 43091933 stop gained G/A snv 4.0E-06 2