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Items: 2

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr16:2126142
GRCh38:
Chr16:2076141
TSC2Tuberous sclerosis 2, Tuberous sclerosis syndromePathogenic
(Nov 1, 2006)
no assertion criteria provided
2.
GRCh37:
Chr16:2126142
GRCh38:
Chr16:2076141
TSC2Tuberous sclerosis 2, Tuberous sclerosis syndrome, not provided
Pathogenic
(Jun 15, 2018)
criteria provided, multiple submitters, no conflicts
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