Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913516
KIT
1.000 0.080 4 54729353 missense variant C/T snv 4.0E-06 6
rs121908586
PDGFRA
1.000 0.080 4 54274869 missense variant T/A;C snv 4
rs121913520
KIT
1.000 0.080 4 54727443 missense variant G/A snv 3
rs17084733
KIT
1.000 0.080 4 54738774 3 prime UTR variant G/A snv 0.10 2
rs778015444
PDGFRA
1.000 0.040 4 54274917 missense variant C/T snv 4.0E-06 7.0E-06 2
rs7909236
CYP2C8
1.000 0.040 10 95069673 upstream gene variant G/T snv 0.18 2
rs1057520031
KIT
1.000 0.040 4 54727440 missense variant A/C;G snv 1
rs1057520033
KIT
1.000 0.040 4 54727439 missense variant G/C snv 1
rs121913523
KIT
1.000 0.040 4 54728092 missense variant T/A;C snv 1
rs1312268347
SARDH
0.925 0.120 9 133734172 start lost A/G snv 5.0E-06 4
rs121913235
KIT
0.925 0.080 4 54727437 missense variant T/A;C;G snv 1
rs397516835
SDHB
0.925 0.080 1 17024040 missense variant C/G;T snv 1
rs1057519711
KIT
0.882 0.240 4 54733168 missense variant T/A snv 4
rs1058930
CYP2C8
0.882 0.040 10 95058362 missense variant G/A;C snv 1.0E-04; 3.7E-02 4
rs764575966
SDHC
0.882 0.080 1 161356832 stop gained C/T snv 3.6E-05 7.0E-06 4
rs587776652
SDHC
0.882 0.200 1 161314408 start lost G/A snv 2
rs201286421
SDHC
0.882 0.080 1 161323636 stop gained C/T snv 8.0E-06 2.1E-05 1
rs786203251
SDHB
0.882 0.080 1 17022649 missense variant G/A;T snv 1
rs917411291
GZMM
0.851 0.360 19 544072 start lost A/C;G snv 9
rs121913512
KIT
0.851 0.120 4 54728055 missense variant A/C;G snv 4
rs750380279
CCDC127 ; SDHA
0.851 0.200 5 218357 start lost T/A;C;G snv 8.7E-06; 8.7E-06 4
rs202101384
SDHB
0.851 0.160 1 17044818 missense variant T/A snv 4.4E-05 1.4E-05 3
rs993022333
KIT
0.851 0.080 4 54733173 missense variant A/C;T snv 3
rs121913517
KIT
0.851 0.120 4 54727444 missense variant T/A;C;G snv 2
rs74315369
SDHB
0.851 0.080 1 17044882 stop gained G/A;C snv 8.0E-06; 4.4E-05 1