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: rs113331868
rs113331868
6 5 150228191 splice donor variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs146838322
rs146838322
1 1 39854058 missense variant A/G snv 1.2E-05 0.700 0
dbSNP: rs1554639173
rs1554639173
3 1.000 9 14120609 frameshift variant TTCGAGTTGAGATG/- delins 0.700 0
dbSNP: rs1554649366
rs1554649366
3 1.000 9 14150191 frameshift variant -/CA delins 0.700 0
dbSNP: rs1554709654
rs1554709654
3 1.000 9 14307156 missense variant A/G snv 0.700 0
dbSNP: rs1554709662
rs1554709662
3 1.000 9 14307175 missense variant T/C snv 0.700 0
dbSNP: rs1554709683
rs1554709683
3 1.000 9 14307210 missense variant T/G snv 0.700 0
dbSNP: rs1554709792
rs1554709792
3 1.000 9 14307442 stop gained G/A snv 0.700 0
dbSNP: rs1554776954
rs1554776954
5 1.000 9 127661133 frameshift variant A/- delins 0.700 0
dbSNP: rs1555928716
rs1555928716
7 0.925 X 20167669 stop gained G/A snv 0.700 0
dbSNP: rs1557739557
rs1557739557
1 1 11114402 missense variant C/T snv 0.700 0
dbSNP: rs1562931936
rs1562931936
5 1.000 7 105107527 stop gained C/T snv 0.700 0
dbSNP: rs730882244
rs730882244
3 1.000 14 35077175 frameshift variant -/A delins 0.700 0
dbSNP: rs764333096
rs764333096
3 1.000 9 14307286 stop gained G/A;T snv 2.0E-05 0.700 0
dbSNP: rs786204927
rs786204927
3 10 87933036 missense variant C/A;G snv 0.700 0
dbSNP: rs869312669
rs869312669
2 1.000 12 13571922 missense variant T/G snv 0.700 0
dbSNP: rs926027867
rs926027867
12 0.882 0.040 5 150251808 missense variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs1555619420
rs1555619420
NF1
3 1.000 0.040 17 31265331 frameshift variant -/G delins 0.700 0
dbSNP: rs1064795760
rs1064795760
14 0.882 0.080 9 92719007 inframe deletion ATT/- del 0.700 0
dbSNP: rs1085308039
rs1085308039
6 0.925 0.080 10 87933075 stop gained G/T snv 0.700 0
dbSNP: rs1085308049
rs1085308049
3 0.925 0.080 10 87957885 stop gained A/T snv 0.700 0
dbSNP: rs1085308053
rs1085308053
5 0.882 0.080 10 87952230 missense variant C/T snv 0.700 0
dbSNP: rs1344172059
rs1344172059
12 0.882 0.080 11 17430838 missense variant C/T snv 7.0E-06 0.700 0
dbSNP: rs1554317931
rs1554317931
11 0.851 0.080 7 42045460 frameshift variant G/- delins 0.700 0
dbSNP: rs1562927768
rs1562927768
15 0.790 0.080 7 105101476 frameshift variant AAAGA/- delins 0.700 0