Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 19
rs1016343
PCAT2 ; PCAT1 ; PRNCR1 ; CASC19
0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20 3
rs10187424
VAMP8
0.925 0.080 2 85567174 intron variant T/A;C snv 2
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 4
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 5
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 1
rs10486567
JAZF1
0.851 0.120 7 27936944 intron variant G/A snv 0.28 2
rs10503733
LOC107986930
0.925 0.080 8 23676505 downstream gene variant G/T snv 0.27 2
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 13
rs10505483
PCAT1 ; CASC19
0.925 0.080 8 127112950 intron variant C/T snv 0.16 2
rs1057519912
MED12
0.776 0.200 X 71129408 missense variant C/G;T snv 5
rs1057519966
LOC107984999 ; SPOP
0.882 0.080 17 49619064 missense variant A/C;T snv 1
rs1057519972
SPOP ; LOC107984999
0.882 0.080 17 49619327 missense variant A/T snv 1
rs1057520005
TP53
0.742 0.360 17 7673800 missense variant C/A;G snv 11
rs1058205
KLK3
0.925 0.080 19 50860142 3 prime UTR variant C/T snv 0.75 0.74 2
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 1
rs10808556
CASC8 ; POU5F1B ; PCAT1 ; CCAT2
0.925 0.080 8 127400902 non coding transcript exon variant C/T snv 0.50 1
rs10875943 0.925 0.080 12 49282227 intergenic variant T/A;C snv 2
rs10896449 0.827 0.200 11 69227200 intergenic variant A/G snv 0.53 3
rs10896450 1.000 0.080 11 69240647 regulatory region variant A/G snv 0.55 1
rs10905371
LOC105376397
1.000 0.080 10 8438081 intron variant A/G snv 0.26 1
rs10905374
LOC105376397
1.000 0.080 10 8439523 intron variant G/A snv 0.25 1
rs10931777
ANKRD44-IT1 ; ANKRD44
1.000 0.080 2 197278867 intron variant C/T snv 0.72 1
rs10934853
EEFSEC
0.882 0.160 3 128319530 intron variant C/A snv 0.43 3
rs10936632 0.925 0.080 3 170412314 intron variant C/A snv 0.41 2