Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 37
rs149617956
MITF
0.672 0.560 3 69964940 missense variant G/A snv 1.4E-03 1.6E-03 32
rs28933406
LRRC56 ; HRAS
0.667 0.480 11 533875 missense variant G/C;T snv 27
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 23
rs142441643
SDHA
0.732 0.320 5 223509 stop gained C/T snv 2.0E-04 2.4E-04 15
rs11214077
SDHD ; TIMM8B
0.752 0.120 11 112087953 missense variant A/G snv 6.6E-03 6.7E-03 12
rs34677591
SDHD ; TIMM8B
0.742 0.120 11 112086941 missense variant G/A snv 7.5E-03 7.0E-03 12
rs80338844
SDHD
0.776 0.280 11 112088939 missense variant C/T snv 2.0E-05 1.4E-05 10
rs772551056
SDHB
0.807 0.120 1 17044824 missense variant C/A;T snv 4.0E-06 9
rs80338845
SDHD
0.807 0.240 11 112088971 missense variant G/T snv 7.0E-06 9
rs587782703
SDHB
0.807 0.160 1 17053947 splice donor variant C/A;T snv 1.2E-05; 4.1E-06 8
rs764575966
SDHC
0.882 0.080 1 161356832 stop gained C/T snv 3.6E-05 7.0E-06 8
rs80338842
TIMM8B ; SDHD
0.790 0.280 11 112086910 start lost G/A;C snv 8
rs587782604
SDHB
0.827 0.120 1 17022684 missense variant C/A;T snv 4.0E-06; 4.0E-06 7
rs876658461
SDHB
0.827 0.200 1 17023975 stop gained G/A snv 7
rs104894309
TIMM8B ; SDHD
0.851 0.200 11 112086940 stop gained C/A;T snv 4.0E-06 7
rs104894304
SDHD
0.827 0.240 11 112094831 missense variant A/G snv 6
rs1064794272
VHL
0.807 0.240 3 10146566 missense variant C/A snv 6
rs201286421
SDHC
0.882 0.080 1 161323636 stop gained C/T snv 8.0E-06 2.1E-05 5
rs104894302
SDHD
0.851 0.200 11 112089002 missense variant A/G;T snv 4.0E-06 5
rs1060503770
SDHD
0.851 0.200 11 112094815 stop gained C/G;T snv 4.0E-06 5
rs1555119834
C11orf65 ; ATM
0.882 0.280 11 108326116 frameshift variant -/T delins 4
rs387906780
SDHA
0.882 0.120 5 251439 missense variant C/T snv 1.2E-05 2.1E-05 4
rs62624461
SDHAF3
0.851 0.080 7 97117880 missense variant T/C snv 2.0E-02 1.8E-02 4
rs786205147
SDHC
0.882 0.120 1 161340638 missense variant G/A;T snv 4