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Results: 3

VariationLocationGene(s)Condition(s)FrequencyClinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr17:45000529
GRCh38:
Chr17:46923163
GOSR2not providedGMAF:0.37320(C)Benign
(Oct 29, 2013)
no assertion criteria provided
2.
GRCh37:
Chr17:45000565
GRCh38:
Chr17:46923199
GOSR2not specified, not providedGMAF:0.01100(A)Benign
(Jan 7, 2015)
criteria provided, single submitter
3.
GRCh37:
Chr17:45000595
GRCh38:
Chr17:46923229
GOSR2not providedGMAF:0.00020(T)Benign
(Feb 6, 2014)
no assertion criteria provided

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