Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918455
PTPN11
0.695 0.440 12 112477720 missense variant A/C;G snv 31
rs137852981
ZEB2
0.752 0.480 2 144399104 stop gained G/A snv 30
rs181109321
TTPA
0.776 0.320 8 63065904 splice region variant C/A;T snv 2.0E-05 15
rs786200952
KAT6A
0.851 0.120 8 41934340 frameshift variant -/T delins 13
rs1563005360
FLNC-AS1 ; FLNC
0.807 0.120 7 128857103 splice acceptor variant ACCTCTGGCCCCCAGGTGTGTCATCAGAGTTCATCGTGAACACCCTGAATGCCGGCTCGGGGGCCTTGTCTGTCACCATTGATGGCCCCTC/GAGG delins 11
rs199473457
KCNQ1
0.827 0.200 11 2572020 missense variant C/A;T snv 11
rs1131692229
KIDINS220
0.851 0.120 2 8730956 frameshift variant GT/- delins 11
rs1057519338
AMMECR1
0.882 X 110264571 stop gained G/A snv 8
rs1565977796
CDK8
0.882 0.120 13 26337623 stop gained C/A snv 7
rs765498367
LOC105373312 ; AMMECR1
0.925 X 110317643 stop gained A/G;T snv 1.2E-04 2.8E-05 6
rs1553196096
CDC42
1 22086463 missense variant G/A snv 5
rs1555447012
NR2F2 ; MIR1469
1.000 15 96332352 stop gained G/T snv 2
rs1566513862
MYH6
14 23400708 splice donor variant C/T snv 1