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Items: 2

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr13:41381515
GRCh38:
Chr13:40807379
SLC25A15Hyperornithinemia-hyperammonemia-homocitrullinuria syndromePathogenic
(May 31, 2012)
no assertion criteria provided
2.
GRCh37:
Chr13:41381539-41381541
GRCh38:
Chr13:40807403-40807405
SLC25A15Hyperornithinemia-hyperammonemia-homocitrullinuria syndromePathogenic
(May 31, 2012)
no assertion criteria provided
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