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Items: 2

VariationLocationGene(s)Condition(s)FrequencyClinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr7:6018306-6018310
GRCh38:
Chr7:5978675-5978679
PMS2Lynch syndrome, Hereditary cancer-predisposing syndromePathogenic
(Sep 5, 2013)
reviewed by expert panel
2.
GRCh37:
Chr3:37067416
GRCh38:
Chr3:37025925
MLH1Lynch syndrome I, Lynch syndrome, Tumor predisposition syndrome
Uncertain significance
(Sep 5, 2013)
reviewed by expert panel