Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 73
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 25
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 22
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 21
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 19
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 18
rs1057941
GBAP1
0.701 0.280 1 155216951 non coding transcript exon variant G/A;T snv 0.46 18
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 18
rs174533
MYRF ; TMEM258
0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 18
rs4808075
BABAM1 ; USHBP1
0.701 0.280 19 17279482 intron variant T/C snv 0.26 18
rs56084662
FRY
0.701 0.280 13 32295727 3 prime UTR variant G/A snv 3.5E-03 18
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21 17
rs11168936
TUBA1C
0.708 0.280 12 49251457 intron variant T/A;C snv 17
rs11200014
FGFR2
0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 17
rs115392158
HLA-B
0.708 0.280 6 31347004 intron variant A/G snv 17
rs11571818
BRCA2
0.708 0.280 13 32394673 intron variant T/C snv 6.6E-03 6.0E-03 17
rs11844632
RAD51B
0.708 0.280 14 68559662 intron variant G/A snv 0.23 17
rs11907546 0.708 0.280 20 34131991 upstream gene variant C/A;T snv 17
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv 17
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs147527678 0.708 0.280 6 32699696 intergenic variant G/A;C snv 17
rs147680653 0.708 0.280 6 29785031 intergenic variant A/G snv 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17