Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs886039799
BBS9
0.763 0.320 7 33273896 frameshift variant C/- del 17
rs121909641
FGFR1
0.763 0.520 8 38419720 missense variant G/A snv 9
rs374434303
PNPLA6
0.882 0.200 19 7561509 missense variant C/A;T snv 3.8E-05 4
rs74452732
UBA6-AS1 ; GNRHR
0.851 0.160 4 67753825 missense variant C/A;T snv 4.0E-06 4
rs1057518936
PNPLA6
0.925 0.120 19 7541025 missense variant C/G snv 3
rs121909628
FGFR1
0.925 0.160 8 38414892 stop gained G/A;C snv 3
rs1363196459
EDNRA
0.882 0.040 4 147486001 missense variant A/G snv 4.0E-06 3
rs28939719
KISS1R
0.882 0.040 19 919563 missense variant T/C snv 3
rs515726224
FGFR1
0.925 0.320 8 38417962 missense variant C/T snv 3
rs727505369
FGFR1
0.925 0.160 8 38424624 missense variant T/C snv 3
rs727505372
TAC3
0.925 0.040 12 57013359 missense variant G/T snv 3
rs727505373
FGFR1
0.925 0.160 8 38429744 missense variant T/C snv 3
rs876661330
FGF8 ; LOC105378457
0.882 0.160 10 101771522 stop gained G/A snv 4.0E-06 3
rs970697573
LPAR2
0.882 0.040 19 19626965 missense variant C/T snv 3
rs104894702
KISS1R
0.925 0.040 19 920746 stop lost T/A;C snv 6.8E-05 2
rs121909640
FGFR1
0.925 0.160 8 38429898 missense variant C/T snv 2
rs121918340
MIR7114 ; NSMF
0.925 0.040 9 137449656 missense variant T/C snv 2
rs606231407
LOC105378457 ; FGF8
1.000 0.040 10 101770613 missense variant C/T snv 1.6E-05 2
rs727505370
FGFR1
1.000 0.040 8 38414840 missense variant A/G snv 2
rs727505371
FGFR1
1.000 0.040 8 38421840 frameshift variant AG/- delins 4.0E-06 2
rs727505374
ANOS1
1.000 0.040 X 8539744 stop gained G/A snv 2
rs727505376
FGFR1
0.925 0.160 8 38414279 missense variant C/G;T snv 2
rs730882248
RNF216 ; MIR6874
0.925 0.160 7 5711761 splice region variant C/T snv 2
rs104893838
GNRHR ; UBA6-AS1
1.000 0.040 4 67753950 missense variant G/A;C;T snv 4.0E-06; 4.0E-06; 1.6E-05 1
rs104893839
GNRHR ; UBA6-AS1
1.000 0.040 4 67744659 missense variant G/T snv 1