Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7959378
TFCP2
1.000 0.080 12 51173447 upstream gene variant A/C snv 0.41 2
rs111904020
STAT3
1.000 0.080 17 42314141 3 prime UTR variant A/C snv 1
rs139394
CBX7
1.000 0.080 22 39142209 intron variant A/C snv 0.70 1
rs1831583
IFNA1
1.000 0.080 9 21439077 upstream gene variant A/C snv 9.5E-03 1
rs2647073
HLA-DRB1
1.000 0.080 6 32606237 intergenic variant A/C snv 0.12 1
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 45
rs4969170
LOC101928674
0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 11
rs1997623
CAV1
0.807 0.160 7 116525306 missense variant A/C;G snv 0.86 9
rs41277434
EZH2
0.851 0.160 7 148809304 splice region variant A/C;G snv 6.8E-02; 8.0E-06 6
rs2239186
VDR
0.882 0.120 12 47875627 intron variant A/C;G snv 0.17 5
rs17006625
KAT2B
0.925 0.080 3 20119604 missense variant A/C;G snv 4.0E-06; 3.3E-02 3
rs3751862
MPHOSPH6
1.000 0.080 16 82148624 3 prime UTR variant A/C;G snv 1
rs3803012
RAN
1.000 0.080 12 130876170 3 prime UTR variant A/C;G snv 1
rs3935401
SDHC
1.000 0.080 1 161363768 3 prime UTR variant A/C;G snv 1
rs455804
GRIK1
1.000 0.080 21 29773850 intron variant A/C;G snv 1
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 98
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 21
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 16
rs121913412
CTNNB1
0.724 0.280 3 41224633 missense variant A/C;G;T snv 9
rs629849
IGF2R
0.827 0.160 6 160073377 missense variant A/C;G;T snv 0.90 0.91 8
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 6
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 5
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 4
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 2
rs1057520006
TP53
0.752 0.240 17 7673799 missense variant A/C;G;T snv 2