Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs750371239
ATM
1.000 0.080 11 108252912 missense variant G/A snv 4.0E-06 1
rs9282655
CDH1
1.000 0.080 16 68823545 missense variant T/C snv 1
rs104886028
KRAS
1.000 0.080 12 25227308 missense variant C/T snv 1
rs121913309
RET
1.000 0.080 10 43120164 inframe deletion TGTTTATGAAGA/- delins 1
rs121913312
RET
1.000 0.080 10 43114494 inframe deletion GAGCTG/- del 1
rs121913313
RET
1.000 0.080 10 43113626 inframe deletion TTCCCTGAGGAGGAGAAGTGCTTCTGC/- delins 1
rs145633958
RET
1.000 0.080 10 43100551 missense variant C/A;T snv 2.7E-03; 4.0E-06 1
rs3026785
RET
1.000 0.080 10 43130238 3 prime UTR variant T/C snv 4.3E-02 1
rs747844360
RET
1.000 0.080 10 43112853 missense variant G/A snv 1.2E-05 1
rs773631693
RET
1.000 0.080 10 43106436 missense variant C/A snv 4.0E-06 1
rs777122776
RET
1.000 0.080 10 43114515 missense variant G/A;T snv 2.8E-05; 4.0E-06 1
rs33927012
SDHB
1.000 0.080 1 17027802 missense variant A/G snv 1.2E-02 9.3E-03 1
rs769177037
SDHC
1.000 0.080 1 161328467 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 1
rs770599902
SDHC
1.000 0.080 1 161362382 missense variant G/A snv 4.0E-06 1
rs864622088
PTCH1
0.925 0.080 9 95459774 missense variant G/T snv 4.0E-06 2
rs2075912
RET
0.925 0.160 10 43126769 3 prime UTR variant T/C snv 0.79 0.84 2
rs2565200
RET
0.925 0.160 10 43127485 3 prime UTR variant T/A;C snv 2
rs377767394
RET
0.925 0.080 10 43113603 missense variant A/C snv 2
rs377767414
RET
0.925 0.080 10 43118397 missense variant G/A snv 2
rs377767415
RET
0.925 0.120 10 43118418 missense variant A/G snv 4.0E-06 2
rs377767426
RET
1.000 0.080 10 43119694 missense variant C/G snv 1.8E-04 1.0E-04 2
rs867966048
SDHC
1.000 0.080 1 161340637 missense variant G/A;C snv 2
rs183334241
TSHZ1
0.925 0.080 18 75288186 missense variant G/A;C snv 1.6E-04 2
rs78081605
TSHZ1
0.925 0.080 18 75288051 missense variant G/C snv 8.0E-06 7.0E-06 2
rs781609053
EGFR
0.925 0.120 7 55200379 missense variant T/C snv 1.2E-05 3