Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs80338796
rs80338796
37 0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 0.700 1.000 2 2007 2007
dbSNP: rs1057519565
rs1057519565
9 0.851 0.200 11 687941 missense variant C/T snv 0.700 1.000 1 2017 2017
dbSNP: rs1554333853
rs1554333853
54 0.689 0.320 7 40046006 missense variant A/G snv 0.700 1.000 1 2017 2017
dbSNP: rs797045141
rs797045141
5 0.882 0.160 15 63696341 splice acceptor variant T/G snv 0.700 1.000 1 2016 2016
dbSNP: rs1057518345
rs1057518345
25 0.742 0.400 20 50894172 frameshift variant ACTA/- delins 0.700 0
dbSNP: rs1057519451
rs1057519451
2 1.000 0.120 14 78709310 missense variant A/G snv 1.4E-05 0.700 0
dbSNP: rs1131691804
rs1131691804
8 0.807 0.200 15 48463123 missense variant G/A snv 0.700 0
dbSNP: rs113871094
rs113871094
34 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
dbSNP: rs1232880706
rs1232880706
36 0.689 0.440 15 48526247 stop gained C/A;T snv 0.700 0
dbSNP: rs137854889
rs137854889
31 0.742 0.440 1 40290871 frameshift variant T/-;TT delins 0.700 0
dbSNP: rs143814221
rs143814221
GHR
8 0.882 0.160 5 42711306 missense variant T/C snv 2.7E-04 2.3E-04 0.700 0
dbSNP: rs1553284997
rs1553284997
17 0.790 0.400 1 92833544 splice acceptor variant G/C snv 0.700 0
dbSNP: rs1555575860
rs1555575860
31 0.732 0.240 16 70496367 missense variant C/G;T snv 0.700 0
dbSNP: rs1567886959
rs1567886959
3 0.882 0.160 17 28534814 frameshift variant C/- delins 0.700 0
dbSNP: rs531047390
rs531047390
2 1.000 0.120 14 78968349 splice region variant A/G snv 2.0E-04 2.1E-05 0.700 0
dbSNP: rs765379963
rs765379963
19 0.701 0.520 1 165743172 stop gained G/A snv 1.2E-05 2.1E-05 0.700 0
dbSNP: rs797045283
rs797045283
11 0.827 0.320 6 157207109 stop gained C/T snv 0.700 0
dbSNP: rs878854402
rs878854402
6 0.851 0.280 3 177033050 missense variant T/C snv 0.700 0
dbSNP: rs886040971
rs886040971
56 0.683 0.280 8 115604339 stop gained G/A;T snv 0.700 0