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Items: 8

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr2:48018275
GRCh38:
Chr2:47791136
MSH6Lynch syndrome, not specified, Hereditary cancer-predisposing syndrome
Likely benign
(Sep 5, 2013)
reviewed by expert panel
2.
GRCh37:
Chr2:48033802-48033805
GRCh38:
Chr2:47806663-47806666
MSH6Hereditary nonpolyposis colorectal cancer type 5, Lynch syndrome, not specified,
Hereditary cancer-predisposing syndrome
Uncertain significance
(Sep 5, 2013)
reviewed by expert panel
3.
GRCh37:
Chr2:48033773-48033776
GRCh38:
Chr2:47806634-47806637
MSH6Lynch syndrome, not provided, Hereditary cancer-predisposing syndrome
Pathogenic
(Sep 5, 2013)
reviewed by expert panel
4.
GRCh37:
Chr2:48027683
GRCh38:
Chr2:47800544
MSH6Lynch syndrome, not specified, Hereditary cancer-predisposing syndrome,
Colorectal cancer
Uncertain significance
(Sep 5, 2013)
reviewed by expert panel
5.
GRCh37:
Chr2:48010533
GRCh38:
Chr2:47783394
MSH6Lynch syndrome, not specified, Hereditary cancer-predisposing syndrome
Likely benign
(Sep 5, 2013)
reviewed by expert panel
6.
GRCh37:
Chr2:48026648
GRCh38:
Chr2:47799509
MSH6Lynch syndrome I, Lynch syndrome, not specified,
not provided, Hereditary cancer-predisposing syndrome
Likely benign
(Sep 5, 2013)
reviewed by expert panel
7.
GRCh37:
Chr2:48025764
GRCh38:
Chr2:47798625
MSH6Lynch syndrome, not specified, Hereditary cancer-predisposing syndrome
Benign
(Sep 5, 2013)
reviewed by expert panel
8.
GRCh37:
Chr2:48027755
GRCh38:
Chr2:47800616
MSH6Hereditary nonpolyposis colorectal cancer type 5, Lynch syndrome, not specified,
not provided, Hereditary cancer-predisposing syndrome, Colorectal / endometrial cancer
Benign
(Sep 5, 2013)
reviewed by expert panel
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