Source: CURATED

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: rs267608078
rs267608078
MSH6 ; FBXO11
0.882 0.160 2 47803501 frameshift variant C/-;CC;CCC delins
CUI: C1333990
Disease: Hereditary Nonpolyposis Colorectal Cancer
Hereditary Nonpolyposis Colorectal Cancer 		0.700 1.000 33 1997 2017
dbSNP: rs267608078
rs267608078
MSH6 ; FBXO11
0.882 0.160 2 47803501 frameshift variant C/-;CC;CCC delins
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.700 1.000 19 1997 2015
dbSNP: rs63750617
rs63750617
MSH6 ; FBXO11
0.851 0.160 2 47803473 missense variant C/G;T snv 4.0E-06; 9.5E-05
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		0.700 1.000 18 2004 2017
dbSNP: rs267608078
rs267608078
MSH6 ; FBXO11
0.882 0.160 2 47803501 frameshift variant C/-;CC;CCC delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		0.700 1.000 16 1997 2017
dbSNP: rs63749873
rs63749873
MSH6 ; FBXO11
0.882 0.160 2 47795903 stop gained C/G snv 4.0E-06 1.4E-05
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		0.700 1.000 14 1999 2015
dbSNP: rs63750767
rs63750767
MSH6 ; FBXO11
0.925 0.160 2 47806588 stop gained -/TCAAAAGGGACATAGAAAA delins 7.0E-06
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.700 1.000 13 2005 2016
dbSNP: rs63751017
rs63751017
MSH6 ; FBXO11
0.851 0.240 2 47800714 stop gained C/A;T snv 1.4E-05
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		0.700 1.000 13 2003 2017
dbSNP: rs2020912
rs2020912
MSH6 ; FBXO11
0.807 0.480 2 47800616 missense variant T/C;G snv 5.1E-03
CUI: C1833477
Disease: COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5 		0.700 1.000 12 1997 2017
dbSNP: rs267608140
rs267608140
MSH6 ; FBXO11
0.925 0.160 2 47806838 missense variant T/A;C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 12 1999 2012
dbSNP: rs34374438
rs34374438
MSH6 ; FBXO11
1.000 0.080 2 47800544 missense variant A/T snv 3.9E-04 3.5E-04
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 12 1999 2012
dbSNP: rs35552856
rs35552856
MSH6 ; FBXO11
1.000 0.160 2 47800166 missense variant A/C;G snv 4.0E-06; 1.2E-05
CUI: C1833477
Disease: COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5 		0.700 1.000 12 1997 2017
dbSNP: rs63749843
rs63749843
MSH6 ; FBXO11
0.827 0.240 2 47803449 stop gained C/A;G;T snv
CUI: C1333990
Disease: Hereditary Nonpolyposis Colorectal Cancer
Hereditary Nonpolyposis Colorectal Cancer 		0.700 1.000 12 2002 2018
dbSNP: rs63749973
rs63749973
MSH6 ; FBXO11
0.925 0.160 2 47799679 stop gained G/A;T snv 2.4E-04 2.8E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 12 1999 2012
dbSNP: rs63749973
rs63749973
MSH6 ; FBXO11
0.925 0.160 2 47799679 stop gained G/A;T snv 2.4E-04 2.8E-05
CUI: C1833477
Disease: COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5 		0.700 1.000 12 1997 2017
dbSNP: rs63750143
rs63750143
MSH6 ; FBXO11
1.000 0.160 2 47791049 missense variant G/A;T snv
CUI: C1833477
Disease: COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5 		0.700 1.000 12 1997 2017
dbSNP: rs63750157
rs63750157
MSH6 ; FBXO11
1.000 0.080 2 47804943 missense variant T/C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 12 1999 2012
dbSNP: rs63750253
rs63750253
MSH6 ; FBXO11
0.925 0.160 2 47803531 missense variant G/A snv 4.8E-05 2.8E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 12 1999 2012
dbSNP: rs63750287
rs63750287
MSH6 ; FBXO11
1.000 0.080 2 47801045 missense variant C/A;G snv 8.4E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 12 1999 2012
dbSNP: rs63750304
rs63750304
MSH6 ; FBXO11
1.000 0.080 2 47800158 missense variant C/G snv 1.6E-05 7.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 12 1999 2012
dbSNP: rs63750358
rs63750358
MSH6 ; FBXO11
1.000 0.080 2 47800037 missense variant G/C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 12 1999 2012
dbSNP: rs63750370
rs63750370
MSH6 ; FBXO11
1.000 0.160 2 47806231 missense variant C/A;T snv 4.0E-06; 7.6E-05
CUI: C1833477
Disease: COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5 		0.700 1.000 12 1997 2017
dbSNP: rs63750389
rs63750389
MSH6 ; FBXO11
0.925 0.160 2 47800532 missense variant A/G snv 8.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 12 1999 2012
dbSNP: rs63750442
rs63750442
MSH6 ; FBXO11
1.000 0.080 2 47803546 missense variant C/G;T snv 7.6E-05; 4.0E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 12 1999 2012
dbSNP: rs63750617
rs63750617
MSH6 ; FBXO11
0.851 0.160 2 47803473 missense variant C/G;T snv 4.0E-06; 9.5E-05
CUI: C1333990
Disease: Hereditary Nonpolyposis Colorectal Cancer
Hereditary Nonpolyposis Colorectal Cancer 		0.700 1.000 12 2006 2017
dbSNP: rs63750617
rs63750617
MSH6 ; FBXO11
0.851 0.160 2 47803473 missense variant C/G;T snv 4.0E-06; 9.5E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 12 1999 2012