Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1553249737
TMCO1
1.000 1 165743263 stop gained G/T snv 4
rs1553631770
CTNNB1
1.000 3 41233398 missense variant A/T snv 4
rs1554200990
GJA1
1.000 6 121446960 missense variant G/C snv 4
rs1554599036
CHD7
1.000 8 60828698 frameshift variant GAACACTGTGGAAGAAC/- del 4
rs1554698878
HNRNPK
0.925 9 83971976 stop gained G/A snv 4
rs1555179320
LOC105369689 ; ABCC9
0.925 0.040 12 21817283 missense variant C/T snv 4
rs1555899177
SON
1.000 21 33554005 frameshift variant ACTC/- del 4
rs1555902810
RBFOX2
1.000 22 35781685 frameshift variant -/A delins 4
rs1555950665
DDX3X ; LOC105373184 ; LOC107985678
1.000 X 41334255 start lost G/C snv 4
rs1556886034
SMC1A
0.925 0.080 X 53382594 missense variant C/T snv 4
rs1557082399
ATRX
1.000 X 77593803 stop gained C/T snv 4
rs387907306
SKI
0.925 0.160 1 2228866 missense variant G/A;T snv 4
rs397507529
PTPN11
0.851 0.160 12 112473031 missense variant A/G snv 7.0E-06 4
rs397518483
RARB
0.851 0.120 3 25596428 missense variant C/A;T snv 4
rs587777357
TUBB
0.925 6 30724263 missense variant G/A snv 4
rs587777695
ZSWIM6
0.925 0.120 5 61544156 missense variant C/T snv 4
rs797044854
ZMYND11
0.925 10 252459 missense variant C/A;T snv 4
rs797044883
MAGEL2
0.882 0.160 15 23645831 stop gained G/A snv 4
rs797044884
PTRH2 ; CLTC
0.925 17 59677123 frameshift variant -/GA delins 4
rs797044885
ZBTB18
0.925 1 244055156 missense variant A/G snv 4
rs864321692
WAC
0.925 10 28583498 stop gained C/A snv 4
rs869025340
BRAF
0.925 0.160 7 140777032 missense variant A/C;G;T snv 4
rs886039392
ITPR1
0.882 0.240 3 4645678 missense variant C/T snv 4
rs886041877
PTEN
1.000 10 87894025 missense variant A/C;G snv 4
rs1045118320
COQ4
0.925 9 128332219 missense variant C/A snv 7.0E-06 3