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Items: 3

VariationLocationGene(s)Condition(s)FrequencyClinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr2:10186419
GRCh38:
Chr2:10046292
KLF11not specifiedGO-ESP:0.09480(G)
GMAF:0.05790(G)
Likely benignno assertion criteria provided
2.
GRCh37:
Chr2:10187874
GRCh38:
Chr2:10047747
KLF11not specifiedGMAF:0.00340(G)Likely benign
(Sep 5, 2013)
criteria provided, single submitter
3.
GRCh37:
Chr2:10187931
GRCh38:
Chr2:10047804
KLF11not providedUncertain significance
(Jun 27, 2013)
criteria provided, single submitter
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