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Items: 4

VariationLocationGene(s)Condition(s)FrequencyClinical significance
(Last reviewed)
Review status
1.
ATP2C1Familial benign pemphigusPathogenic
(Jan 1, 2000)
no assertion criteria provided
2.
GRCh37:
Chr3:130688229
GRCh38:
Chr3:130969385
ATP2C1Familial benign pemphigusPathogenic
(Jan 1, 2000)
no assertion criteria provided
3.
GRCh37:
Chr3:130682825
GRCh38:
Chr3:130963981
ATP2C1Familial benign pemphigusPathogenic
(Jan 1, 2000)
no assertion criteria provided
4.
ATP2C1Familial benign pemphigusPathogenic
(Jan 1, 2000)
no assertion criteria provided
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