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Items: 2

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr2:128186468
GRCh38:
Chr2:127428892
PROCThrombophilia, hereditary, due to protein C deficiency, autosomal dominantPathogenic
(May 1, 1987)
no assertion criteria provided
2.
GRCh37:
Chr2:128186178
GRCh38:
Chr2:127428602
PROCThrombophilia, hereditary, due to protein C deficiency, autosomal dominantPathogenic
(Aug 1, 1992)
no assertion criteria provided
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