Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587781351
CDH1
1.000 0.040 16 68828263 missense variant G/A;C snv 4.0E-06; 4.0E-06 2
rs866551255
CDKN1A
1.000 0.040 6 36684145 missense variant G/A snv 2
rs1390902532
CDKN2A
1.000 0.040 9 21968766 missense variant T/C snv 7.4E-06 7.0E-06 2
rs1356083197
CNIH3 ; WDR26
1.000 0.040 1 224434068 missense variant C/T snv 1.5E-05 1.4E-05 2
rs373646414
DICER1
1.000 0.080 14 95132574 missense variant T/C snv 1.6E-05 5.6E-05 2
rs2279398
DOK3
1.000 0.080 5 177503768 3 prime UTR variant C/T snv 2.7E-02 2
rs1457127715
ERBB2
17 39715810 missense variant G/A;C snv 4.0E-06 2
rs761896295
FGFR3
1.000 0.080 4 1804450 missense variant G/A snv 2.4E-05 2.1E-05 2
rs750949764
FOS
1.000 0.040 14 75280958 missense variant G/C snv 4.0E-06 2
rs538912281
FOXE1 ; PTCSC2
0.925 0.080 9 97854657 missense variant C/A;G;T snv 2.0E-03 2
rs751478142
HSPA9 ; LOC105379193
1.000 5 138570994 missense variant G/A snv 2.8E-05 1.4E-05 2
rs11777210
KBTBD11
1.000 0.080 8 1979843 intron variant C/G;T snv 2
rs868438023
KNSTRN
0.882 0.080 15 40382906 missense variant C/T snv 2
rs57408770
MIR3131 ; IHH
1.000 0.080 2 219058688 non coding transcript exon variant -/AAG delins 2
rs28933369
MIR4728 ; ERBB2
0.925 0.080 17 39724744 missense variant G/A snv 2
rs760583024
MRGPRX1
1.000 0.080 11 18934156 missense variant G/A;T snv 8.0E-06 2
rs1374712964
MUTYH
1.000 0.080 1 45332028 missense variant T/C snv 2
rs1670661
NELL1
1.000 0.040 11 21209124 intron variant C/G;T snv 2
rs113561019
OGG1
1.000 0.080 3 9756791 missense variant G/A;T snv 3.9E-03; 4.0E-06 2
rs1400826115
OGG1
1.000 0.080 3 9756770 missense variant A/G snv 4.0E-06 2
rs200817352
PAX8 ; PAX8-AS1
1.000 0.080 2 113220126 missense variant G/A;C snv 2.0E-03; 4.0E-06 2
rs104893859
PITX2
0.925 0.080 4 110618669 missense variant C/G;T snv 2
rs28936409
PITX2
1.000 0.080 4 110621303 missense variant C/A;G;T snv 4.0E-06; 8.0E-06 2
rs771308693
PTK2
8 140752306 missense variant G/A snv 3.2E-05 7.0E-06 2
rs13254990
PVT1
0.882 0.120 8 128064205 intron variant C/T snv 0.24 2