Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 10
rs769240800
PALB2
0.925 0.120 16 23638116 stop gained A/C snv 8.0E-06 3
rs11814448 0.925 0.080 10 22026914 intergenic variant A/C snv 0.21 2
rs3734805
CCDC170 ; LOC107986528
0.925 0.080 6 151618215 3 prime UTR variant A/C snv 6.9E-02 2
rs6815814
TLR1
1.000 0.080 4 38814717 intron variant A/C snv 0.43 2
rs9693444 0.925 0.080 8 29652100 intergenic variant A/C snv 0.66 2
rs12048493
OTUD7B
1.000 0.080 1 149955122 intron variant A/C snv 0.29 1
rs12918713 1.000 0.080 16 10609831 regulatory region variant A/C snv 5.8E-02 1
rs149936356
LOC101929594 ; TTC28
1.000 0.080 22 28532870 intron variant A/C snv 1.8E-02 1
rs17001868
ADSL ; SGSM3 ; LOC107985538
0.925 0.080 22 40382227 intron variant A/C snv 0.12 1
rs17489300
LGR6
1.000 0.080 1 202209914 intron variant A/C snv 0.31 1
rs17598658
H2BC6
1.000 0.080 6 26175638 intron variant A/C snv 4.8E-02 1
rs2253762
TACC2
1.000 0.080 10 122041907 intron variant A/C snv 0.32 1
rs2296135
IL15RA
0.851 0.080 10 5952731 3 prime UTR variant A/C snv 0.58 1
rs2724379
CD34
1.000 0.080 1 207903511 intron variant A/C snv 0.24 1
rs2787486
STXBP4
0.925 0.080 17 55132413 intron variant A/C snv 0.33 1
rs6180
GHR
0.827 0.160 5 42719137 missense variant A/C snv 0.44 0.43 1
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 15
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 8
rs80356959
BRCA1
0.851 0.200 17 43045761 missense variant A/C;G snv 4
rs11249433
EMBP1
0.827 0.160 1 121538815 intron variant A/C;G snv 3
rs7107217 0.882 0.160 11 129603795 intron variant A/C;G snv 3
rs12286929 0.925 0.080 11 115151684 intergenic variant A/C;G snv 2
rs280519
TYK2
0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 2
rs11196174
TCF7L2
1.000 0.080 10 112974337 intron variant A/C;G snv 1