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Items: 5

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr2:47703500
GRCh38:
Chr2:47476361
MSH2Lynch syndrome I, Lynch syndrome, not specified,
Hereditary cancer-predisposing syndrome
Benign
(Sep 5, 2013)
reviewed by expert panel
2.
GRCh37:
Chr2:47702319
GRCh38:
Chr2:47475180
MSH2Lynch syndrome I, Lynch syndrome, not provided,
Hereditary cancer-predisposing syndrome
Pathogenic
(Sep 5, 2013)
reviewed by expert panel
3.
GRCh37:
Chr2:47657020
GRCh38:
Chr2:47429881
MSH2Lynch syndrome I, Lynch syndrome, not provided,
Hereditary cancer-predisposing syndrome, Hereditary nonpolyposis colon cancer
Pathogenic
(Sep 5, 2013)
reviewed by expert panel
4.
MSH2Lynch syndrome IPathogenic
(Dec 17, 1993)
no assertion criteria provided
5.
GRCh37:
Chr2:47702269
GRCh38:
Chr2:47475130
MSH2Lynch syndrome I, Lynch syndrome, Hereditary cancer-predisposing syndrome
Pathogenic
(Sep 5, 2013)
reviewed by expert panel
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