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: rs63750339
rs63750339
MLH1
0.925 0.200 3 37020441 frameshift variant C/- delins
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2019 2019
dbSNP: rs63750339
rs63750339
MLH1
0.925 0.200 3 37020441 frameshift variant C/- delins
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2019 2019
dbSNP: rs63750339
rs63750339
MLH1
0.925 0.200 3 37020441 frameshift variant C/- delins
CUI: C0262401
Disease: Carcinoma of ampulla of Vater
Carcinoma of ampulla of Vater 		0.010 1.000 1 2019 2019