Source: ALL
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: rs1085308056
rs1085308056
PTEN
8 0.851 0.160 10 87957850 splice region variant C/G snv 0.700 0
dbSNP: rs1131692245
rs1131692245
NPHS1
7 0.925 0.160 19 35844109 missense variant C/T snv 0.700 0
dbSNP: rs1163944538
rs1163944538
TMEM94
73 0.641 0.560 17 75494905 frameshift variant -/A delins 4.0E-06 0.700 0
dbSNP: rs1178187217
rs1178187217
DNAH11
38 0.683 0.480 7 21600085 missense variant G/A;T snv 4.3E-06 0.700 0
dbSNP: rs121909218
rs121909218
PTEN
25 0.672 0.360 10 87933145 missense variant G/A snv 0.700 0
dbSNP: rs121909219
rs121909219
PTEN
25 0.689 0.400 10 87957915 stop gained C/A;T snv 0.700 0
dbSNP: rs121909224
rs121909224
PTEN
41 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 0.700 0
dbSNP: rs121909231
rs121909231
PTEN
32 0.667 0.600 10 87961095 stop gained C/A;T snv 0.700 0
dbSNP: rs121913293
rs121913293
PTEN
18 0.732 0.360 10 87952142 missense variant C/A;T snv 0.700 0
dbSNP: rs121913294
rs121913294
PTEN
14 0.776 0.280 10 87952143 missense variant G/A;C;T snv 8.0E-06 0.700 0
dbSNP: rs121913355
rs121913355
BRAF
42 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 0.700 0
dbSNP: rs1232880706
rs1232880706
FBN1
36 0.689 0.440 15 48526247 stop gained C/A;T snv 0.700 0
dbSNP: rs1344172059
rs1344172059
ABCC8
12 0.882 0.080 11 17430838 missense variant C/T snv 7.0E-06 0.700 0
dbSNP: rs1352010373
rs1352010373
TMEM94
73 0.641 0.560 17 75489265 splice acceptor variant G/C snv 0.700 0
dbSNP: rs141322087
rs141322087
ABCC8
13 0.851 0.160 11 17404552 missense variant C/T snv 1.2E-05 2.1E-05 0.700 0
dbSNP: rs146838322
rs146838322
TRIT1
1 1 39854058 missense variant A/G snv 1.2E-05 0.700 0
dbSNP: rs1553544133
rs1553544133
SATB2
6 0.851 0.200 2 199308845 frameshift variant TC/- delins 0.700 0
dbSNP: rs1554121443
rs1554121443
SYNGAP1 ; MIR5004
29 0.742 0.280 6 33438873 stop gained C/T snv 0.700 0
dbSNP: rs1554317931
rs1554317931
GLI3
11 0.851 0.080 7 42045460 frameshift variant G/- delins 0.700 0
dbSNP: rs1554639173
rs1554639173
NFIB
3 1.000 9 14120609 frameshift variant TTCGAGTTGAGATG/- delins 0.700 0
dbSNP: rs1554649366
rs1554649366
NFIB
3 1.000 9 14150191 frameshift variant -/CA delins 0.700 0
dbSNP: rs1554709654
rs1554709654
NFIB
3 1.000 9 14307156 missense variant A/G snv 0.700 0
dbSNP: rs1554709662
rs1554709662
NFIB
3 1.000 9 14307175 missense variant T/C snv 0.700 0
dbSNP: rs1554709683
rs1554709683
NFIB
3 1.000 9 14307210 missense variant T/G snv 0.700 0
dbSNP: rs1554709792
rs1554709792
NFIB
3 1.000 9 14307442 stop gained G/A snv 0.700 0