Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs786202998
BRCA1
0.851 0.080 17 43091030 stop gained C/A;T snv 5
rs80356880
BRCA1
0.851 0.080 17 43115750 missense variant G/C;T snv 5
rs9306160
RRP1B
0.925 0.080 21 43687681 missense variant T/C snv 0.69 0.73 5
rs10109984
PRKDC
0.925 0.080 8 47891114 intron variant T/C snv 0.54 4
rs10235235
ZNF394 ; ZNF789
0.925 0.080 7 99478208 intron variant T/C snv 0.13 4
rs1053872
RCL1
0.925 0.080 9 4860643 3 prime UTR variant G/C;T snv 4
rs1056123575
ADAMTS1
0.925 0.080 21 26844557 missense variant G/A snv 4.2E-06 7.0E-06 4
rs1062577
ESR1
0.882 0.080 6 152102770 3 prime UTR variant T/A;G snv 4
rs1064793184
FBXO11 ; MSH6
0.851 0.080 2 47791055 missense variant A/G snv 4
rs10822013
ZNF365
0.851 0.080 10 62492218 intron variant C/T snv 0.42 4
rs10995190
ZNF365
0.882 0.080 10 62518923 intron variant G/A snv 0.16 4
rs1114167795
FBXO11 ; MSH6
0.851 0.080 2 47799482 missense variant C/T snv 4
rs11552449
AP4B1 ; DCLRE1B
0.925 0.080 1 113905767 missense variant C/G;T snv 0.22 0.15 4
rs1172398253
CCN1
0.925 0.080 1 85582045 missense variant C/T snv 4.0E-06 4
rs11780156
PVT1
0.925 0.080 8 128182395 intron variant C/T snv 0.13 4
rs11895168
ERBB4
0.925 0.080 2 211377467 3 prime UTR variant A/C snv 0.68 4
rs121917739
RAD51
0.882 0.080 15 40718818 missense variant G/A snv 3.7E-04 1.7E-03 4
rs12286929 0.925 0.080 11 115151684 intergenic variant A/C;G snv 4
rs12662670
CCDC170
0.851 0.080 6 151597721 intron variant T/C;G snv 4
rs1292011
LOC105370003
0.851 0.080 12 115398717 regulatory region variant A/G snv 0.43 4
rs12945597
TOP3A
0.925 0.080 17 18271367 downstream gene variant G/A snv 0.31 4
rs13000023
LOC101928278 ; LOC105373873
0.851 0.080 2 217059671 downstream gene variant G/A;C;T snv 0.19 4
rs13283662
UHRF2
0.925 0.080 9 6428530 intron variant T/C snv 4
rs1364963022
ESR1
0.925 0.080 6 151944233 missense variant G/C snv 4.0E-06 4
rs141613848
SLC9A3R1
0.925 0.080 17 74768481 missense variant A/T snv 1.0E-03 1.2E-03 4