MYH10, myosin heavy chain 10, 4628

N. diseases: 31; N. variants: 1
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: rs2270744
rs2270744 		1.000 0.080 17 8490582 intron variant G/C snv 0.36 0.35
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs2270744
rs2270744 		1.000 0.080 17 8490582 intron variant G/C snv 0.36 0.35
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs2270744
rs2270744 		1.000 0.080 17 8490582 intron variant G/C snv 0.36 0.35
CUI: C0035335
Disease: Retinoblastoma
Retinoblastoma 		Neoplasms; Eye Diseases 0.010 1.000 1 2016 2016