Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267607165
TUBB3
0.708 0.520 16 89935679 missense variant G/A;C snv 18
rs121909636
FGFR1
0.827 0.240 8 38414569 stop gained G/A snv 7
rs397515445
FGFR1
0.807 0.280 8 38414263 missense variant T/C snv 7
rs121909635
FGFR1
0.827 0.240 8 38426158 missense variant C/T snv 6
rs267606805
FGFR1
0.851 0.240 8 38414173 missense variant G/T snv 5
rs267606806
FGFR1
0.851 0.240 8 38414166 missense variant G/A;C snv 1.2E-05 5
rs121909173
HESX1
0.851 0.240 3 57199901 missense variant C/G snv 2.8E-05 1.4E-05 5
rs1306416169
NSMF
0.851 0.280 9 137453808 missense variant C/T snv 5
rs1487309678
SEMA3A
0.851 0.280 7 84014246 missense variant C/T snv 8.0E-06 5
rs1269636220
WDR11
0.851 0.280 10 120865109 missense variant A/G snv 5
rs572007403
KISS1R
0.882 0.200 19 919955 missense variant C/A snv 3.3E-04 9.1E-05 4
rs78861628
PROKR2
0.851 0.160 20 5302393 missense variant G/A snv 3.9E-03 1.4E-02 4
rs137852660
FGF8
0.882 0.160 10 101775209 missense variant G/A snv 1.1E-03 8.0E-04 3
rs137852515
ANOS1
0.925 0.160 X 8536852 missense variant C/T snv 2
rs587777863
PROK2 ; LOC105377156
0.925 0.160 3 71784983 missense variant C/G snv 7.0E-06 2
rs138672528
PROKR2
0.925 0.160 20 5314027 missense variant C/T snv 3.2E-05 7.0E-06 2
rs202203360
PROKR2
0.925 0.160 20 5314033 missense variant A/G snv 1.2E-04 3.5E-05 2
rs369831329
PROKR2
0.925 0.160 20 5302374 missense variant A/T snv 8.0E-06 2
rs199979628
SEMA3A
0.925 0.160 7 84134868 missense variant G/A snv 5.3E-04 4.3E-04 2
rs2229013
ANOS1
1.000 0.160 X 8535755 missense variant C/A;T snv 8.7E-04 1
rs141929169
AXL
1.000 0.160 19 41238557 missense variant A/C snv 1.5E-03 1.4E-03 1
rs374447937
EGR1
1.000 0.160 5 138465831 missense variant C/G snv 4.0E-06 1
rs1126485
FGFR1
1.000 0.160 8 38424522 missense variant A/G snv 1
rs1424371425
FGFR1
1.000 0.160 8 38461099 frameshift variant -/C delins 7.4E-05 4.2E-05 1
rs199573818
FGFR1
1.000 0.160 8 38417882 missense variant T/C;G snv 1