Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 33
rs79658334
RET
0.662 0.360 10 43119548 missense variant G/A;C;T snv 1.2E-04; 4.3E-06 29
rs75076352
RET
0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 24
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 23
rs75996173
RET
0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 21
rs76262710
RET
0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 17
rs79781594
RET
0.732 0.160 10 43113649 missense variant G/A;C;T snv 16
rs77939446
RET
0.724 0.120 10 43113622 missense variant G/A;C;T snv 4.0E-06 15
rs75234356
RET
0.716 0.240 10 43120144 missense variant T/G snv 1.2E-05 7.0E-06 14
rs77709286
RET
0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 12
rs78014899
RET
0.742 0.160 10 43118392 missense variant G/A;C;T snv 8.0E-06 12
rs377767404
RET
0.742 0.160 10 43114488 missense variant T/C snv 11
rs77503355
RET
0.776 0.160 10 43113655 missense variant G/A;C;T snv 8
rs377767429
RET
0.790 0.120 10 43120120 missense variant GC/TT mnv 7
rs121917832
GPR19 ; CDKN1B
0.925 0.200 12 12718066 stop gained G/A snv 3
rs774454456
GPR19 ; CDKN1B
0.925 0.120 12 12717808 5 prime UTR variant AGAG/- delins 3.8E-04 3.8E-04 2
rs777354267
GPR19 ; CDKN1B
1.000 0.120 12 12718045 missense variant C/T snv 4.0E-06 2.1E-05 2
rs1060500186
CDKN1B ; GPR19
1.000 0.120 12 12717887 frameshift variant GACG/- delins 1
rs1555085575
CDKN1B ; GPR19
1.000 0.120 12 12718118 frameshift variant -/C delins 1
rs532903617
CDKN1B ; GPR19
1.000 0.120 12 12718106 stop gained C/G;T snv 4.0E-06 1.4E-05 1
rs786201007
CDKN1B ; GPR19
1.000 0.120 12 12717896 frameshift variant -/AGGCGGAGCACCCCAAGCC delins 1
rs786201011
CDKN1B ; GPR19
1.000 0.120 12 12718211 frameshift variant CT/- delins 1
rs786201010
GPR19 ; CDKN1B
1.000 0.120 12 12717384 5 prime UTR variant TTCC/- delins 1