Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs75002266
ORC4
0.827 0.160 2 147939241 missense variant G/A snv 3.2E-03 3.0E-03 6
rs1242982981
CLEC12A
0.851 0.160 12 9984989 missense variant C/T snv 4
rs6535455
HPSE
0.851 0.160 4 83310951 intron variant T/A;C snv 4
rs1934951
CYP2C8
0.925 0.160 10 95038791 intron variant C/T snv 0.24 3
rs1052501
ULK4
0.925 0.160 3 41883906 missense variant C/G;T snv 0.80 2
rs12717
TBP ; PSMB1
0.925 0.160 6 170553212 missense variant G/C snv 0.42 0.38 2
rs2285803
PSORS1C2 ; PSORS1C1
0.925 0.160 6 31139481 intron variant T/C snv 0.72 2
rs4273077
TNFRSF13B
0.925 0.160 17 16945825 intron variant A/G snv 0.13 2
rs6768972
CRBN
1.000 0.160 3 3180101 upstream gene variant A/C;G snv 2
rs756168629
LRP1B
1.000 0.160 2 140841050 missense variant C/T snv 4.8E-05 1.4E-05 2
rs1045433
TRNT1 ; CRBN
1.000 0.160 3 3149742 non coding transcript exon variant T/C snv 0.15 1
rs1049633
DDR1
1.000 0.160 6 30899750 3 prime UTR variant G/A snv 7.6E-02 1
rs1057519718
BRAF
0.925 0.160 7 140753355 missense variant CA/TC mnv 1
rs11064392
CD4
1.000 0.160 12 6789226 intron variant A/G snv 0.14 1
rs12374648
LOC102723831
1.000 0.160 6 151208234 intron variant A/G snv 0.22 1
rs1250801605
CASP10
1.000 0.160 2 201185809 missense variant G/A snv 4.0E-06 1
rs13409
POU5F1 ; TCF19
1.000 0.160 6 31164363 3 prime UTR variant G/A snv 0.44 1
rs143267032
CUX1
1.000 0.160 7 102028117 missense variant C/G snv 2.8E-05 2.8E-05 1
rs1450703683
ANOS1
1.000 0.160 X 8533018 missense variant T/C snv 1.9E-05 1
rs145738773
CASP9
1.000 0.160 1 15504663 synonymous variant G/A snv 4.4E-05 1.0E-04 1
rs1555902 1.000 0.160 13 108204435 downstream gene variant C/A snv 0.10 1
rs193451 1.000 0.160 7 108670542 intergenic variant A/G snv 0.36 1
rs210143
GGNBP1 ; BAK1
0.827 0.160 6 33579153 intron variant T/C snv 0.74 1
rs3777189
ELL2
1.000 0.160 5 95917404 intron variant C/G snv 0.34 1
rs3815768
ELL2
1.000 0.160 5 95900755 missense variant C/T snv 0.27 0.29 1