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Results: 2

VariationLocationGene(s)Condition(s)FrequencyClinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr2:29296527
GRCh38:
Chr2:29073661
C2orf71Retinitis pigmentosa 54Pathogenic
(Jun 26, 2015)
no assertion criteria provided
2.
C2orf71Retinitis pigmentosa 54Pathogenic
(Sep 9, 2010)
no assertion criteria provided