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: rs314276
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2012 2012
dbSNP: rs314276
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		0.010 1.000 1 2014 2014
dbSNP: rs314276
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65
CUI: C0205770
Disease: Choroid Plexus Papilloma
Choroid Plexus Papilloma 		0.010 1.000 1 2017 2017
dbSNP: rs314276
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2012 2012
dbSNP: rs314276
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial 		0.010 1.000 1 2012 2012
dbSNP: rs314276
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65
CUI: C1333015
Disease: Childhood Kidney Wilms Tumor
Childhood Kidney Wilms Tumor 		0.010 1.000 1 2018 2018
dbSNP: rs314276
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma 		0.010 1.000 1 2018 2018
dbSNP: rs314276
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65
CUI: C0677886
Disease: Epithelial ovarian cancer
Epithelial ovarian cancer 		0.010 1.000 1 2012 2012