rs3087468, NTHL1

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Congenital chromosomal disease
CUI: C0008626
Disease: Congenital chromosomal disease
47 16 2040233 missense variant C/A snv 0.010 1.000 1 2013 2013
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 16 2040233 missense variant C/A snv 0.010 1.000 1 2013 2013
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 16 2040233 missense variant C/A snv 0.010 1.000 1 2013 2013