Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1555187633
SDHD
1.000 0.040 11 112094933 missense variant G/T snv 1
rs899706404
SDHD ; TIMM8B
0.925 0.040 11 112087944 missense variant A/G snv 3
rs1208512558
POMC
0.925 0.040 2 25161623 missense variant C/G;T snv 6.7E-06 2
rs1265416900
CHGA
0.925 0.040 14 92932783 missense variant C/T snv 2
rs1456371000
CHGA
0.925 0.040 14 92931642 missense variant C/T snv 2
rs776485432
SDHC
0.925 0.040 1 161356764 missense variant C/A;T snv 4.0E-06 2
rs764575966
SDHC
0.882 0.080 1 161356832 stop gained C/T snv 3.6E-05 7.0E-06 8
rs201286421
SDHC
0.882 0.080 1 161323636 stop gained C/T snv 8.0E-06 2.1E-05 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
rs786205147
SDHC
0.882 0.120 1 161340638 missense variant G/A;T snv 4
rs1449052677
POMC
0.882 0.120 2 25161643 missense variant T/C snv 1.3E-05 3
rs80338846
SDHD
0.882 0.080 11 112088981 missense variant T/C snv 3
rs80338847
SDHD
0.882 0.200 11 112094906 missense variant T/C;G snv 3
rs942160050
SDHC
0.882 0.080 1 161356685 missense variant C/A;G;T snv 4.0E-06 3
rs104894309
TIMM8B ; SDHD
0.851 0.200 11 112086940 stop gained C/A;T snv 4.0E-06 7
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
rs1420960657
SDHD
0.851 0.080 11 112093192 missense variant A/G snv 4
rs62624461
SDHAF3
0.851 0.080 7 97117880 missense variant T/C snv 2.0E-02 1.8E-02 4
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
rs104894304
SDHD
0.827 0.240 11 112094831 missense variant A/G snv 6
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