Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs57961569
rs57961569
MYCN ; MYCNOS
0.827 0.200 2 15939643 intron variant G/A;C snv
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma 		0.010 1.000 1 2018 2018
dbSNP: rs57961569
rs57961569
MYCN ; MYCNOS
0.827 0.200 2 15939643 intron variant G/A;C snv
CUI: C4086165
Disease: Childhood Neuroblastoma
Childhood Neuroblastoma 		0.010 1.000 1 2018 2018
dbSNP: rs57961569
rs57961569
MYCN ; MYCNOS
0.827 0.200 2 15939643 intron variant G/A;C snv
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma 		0.010 1.000 1 2018 2018
dbSNP: rs57961569
rs57961569
MYCN ; MYCNOS
0.827 0.200 2 15939643 intron variant G/A;C snv
CUI: C1333015
Disease: Childhood Kidney Wilms Tumor
Childhood Kidney Wilms Tumor 		0.010 1.000 1 2019 2019
dbSNP: rs57961569
rs57961569
MYCN ; MYCNOS
0.827 0.200 2 15939643 intron variant G/A;C snv
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma 		0.010 1.000 1 2019 2019