Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1991517
LOC101928462 ; TSHR
0.752 0.240 14 81144239 missense variant G/C snv 0.90 0.91 13
rs57920071
LMNA
0.763 0.320 1 156136984 missense variant C/T snv 4.0E-06 7.0E-06 11
rs886037704
DICER1
0.925 0.080 14 95103856 stop gained G/T snv 3
rs537209983
NKX2-1 ; NKX2-1-AS1 ; SFTA3
0.882 0.080 14 36517378 missense variant G/A snv 1.7E-04 8.4E-05 3
rs2234919
TSHR ; CEP128
0.925 0.160 14 80955834 missense variant C/A;G snv 6.8E-02; 1.2E-05 2
rs1284307491
PTCSC2 ; FOXE1
1.000 0.080 9 97854332 missense variant G/C snv 4.2E-06 1