Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199472961
KCNH2
0.925 0.120 7 150951495 missense variant T/A;C snv 2
rs199472978
KCNH2
0.925 0.120 7 150951097 missense variant C/A;G;T snv 2
rs199472983
KCNH2
0.925 0.120 7 150950988 missense variant A/G snv 2
rs199472986
KCNH2
0.925 0.120 7 150950404 missense variant G/A snv 2
rs199472997
KCNH2
0.925 0.120 7 150950204 missense variant C/T snv 2
rs199472999
KCNH2
0.925 0.120 7 150949034 missense variant A/C;G snv 2
rs199473000
KCNH2
1.000 0.120 7 150949031 missense variant C/G;T snv 2
rs199473004
KCNH2
0.925 0.120 7 150948938 missense variant T/C snv 2
rs199473005
KCNH2
0.925 0.120 7 150948939 missense variant C/A;T snv 2
rs199473419
KCNH2
0.925 0.120 7 150974809 missense variant T/C snv 2
rs199473421
KCNH2
0.925 0.120 7 150974803 missense variant G/A;C;T snv 2
rs199473430
KCNH2
0.925 0.120 7 150951638 missense variant C/A;G snv 2
rs199473487
KCNH2
0.925 0.120 7 150974920 missense variant T/G snv 2
rs199473506
KCNH2
0.925 0.120 7 150952777 missense variant T/C snv 2
rs199473507
KCNH2
0.925 0.120 7 150952723 missense variant T/C snv 2
rs199473524
KCNH2
0.925 0.120 7 150951555 missense variant G/A snv 2
rs28928904
KCNH2
0.925 0.120 7 150951615 missense variant A/C;G;T snv 4.0E-06 2
rs587777907
KCNH2
1.000 0.120 7 150958319 missense variant T/A snv 2.0E-05 2
rs730880116
KCNH2
0.925 0.120 7 150958290 stop gained C/A snv 2
rs761863251
KCNH2
0.925 0.120 7 150959591 frameshift variant G/-;GG delins 2
rs77331749
KCNH2
0.925 0.120 7 150947833 missense variant G/A snv 4.0E-04 5.5E-04 2
rs794728382
KCNH2
0.925 0.120 7 150950962 stop gained G/A snv 2
rs794728391
KCNH2
0.925 0.120 7 150950167 splice donor variant C/A;G snv 2
rs972201049
KCNH2
0.925 0.120 7 150955481 missense variant G/A snv 3.3E-05 2.1E-05 2
rs1131692183
KCNH2
1.000 0.120 7 150948456 frameshift variant -/CCTGC delins 1