Source: CLINVAR

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: rs267608120
rs267608120
MSH6 ; FBXO11
0.925 0.160 2 47806606 frameshift variant CAAG/- delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		0.700 1.000 9 2003 2014
dbSNP: rs267608120
rs267608120
MSH6 ; FBXO11
0.925 0.160 2 47806606 frameshift variant CAAG/- delins
CUI: C1333990
Disease: Hereditary Nonpolyposis Colorectal Cancer
Hereditary Nonpolyposis Colorectal Cancer 		0.700 1.000 8 2003 2015
dbSNP: rs267608120
rs267608120
MSH6 ; FBXO11
0.925 0.160 2 47806606 frameshift variant CAAG/- delins
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.700 1.000 8 2003 2016
dbSNP: rs267608120
rs267608120
MSH6 ; FBXO11
0.925 0.160 2 47806606 frameshift variant CAAG/- delins
CUI: C1833477
Disease: COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5 		0.700 1.000 3 2003 2011