Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs150766139
NTHL1 ; TSC2
0.742 0.320 16 2046238 stop gained G/A snv 1.4E-03 1.4E-03 13
rs4968451
BRIP1
0.732 0.160 17 61849946 intron variant A/C snv 0.15 13
rs768803947
TP53
0.882 0.080 17 7670624 missense variant C/A;T snv 4.0E-06; 4.0E-06 3
rs1035938
BICRA
0.776 0.120 19 47680514 missense variant C/G;T snv 0.29 8
rs25406
PCNA-AS1 ; PCNA
0.807 0.120 20 5118990 intron variant G/A snv 0.41 8