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Items: 2

VariationLocationGene(s)Condition(s)FrequencyClinical significance
(Last reviewed)
Review status
1.
GRCh37:
ChrX:110406205
GRCh38:
ChrX:111162977
PAK3not specifiedGMAF:0.00210(A)Uncertain significance
(Aug 12, 2014)
criteria provided, single submitter
2.
GRCh37:
ChrX:110439144
GRCh38:
ChrX:111195916
PAK3not specifiedGO-ESP:0.01316(T)
GMAF:0.00900(T)
Likely benignno assertion criteria provided
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