rs1131691041, TP53

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.
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 17 7676271 frameshift variant -/A delins 0.700 0
Congenital chromosomal disease
CUI: C0008626
Disease: Congenital chromosomal disease
47 17 7676271 frameshift variant -/A delins 0.010 1.000 1 2017 2017
MYELODYSPLASTIC SYNDROME
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
95 17 7676271 frameshift variant -/A delins 0.010 1.000 1 2017 2017