MYO10, myosin X, 4651

N. diseases: 34; N. variants: 9
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11133865
rs11133865
5 16854596 intron variant T/C snv 0.30
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
0.700 1.000 1 2018 2018
dbSNP: rs13361131
rs13361131
5 16804871 intron variant A/G snv 6.1E-02
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
0.700 1.000 1 2018 2018
dbSNP: rs17651415
rs17651415
5 16858112 intron variant A/G snv 0.14
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
0.700 1.000 1 2018 2018
dbSNP: rs2625206
rs2625206
5 16858173 intron variant T/A;C snv 0.39
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
0.700 1.000 1 2018 2018
dbSNP: rs7719940
rs7719940
5 16852625 intron variant T/C snv 0.33
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
0.700 1.000 1 2018 2018
dbSNP: rs7736840
rs7736840
5 16856090 intron variant T/C snv 0.30
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
0.700 1.000 1 2018 2018