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Items: 2

VariationLocationGene(s)Condition(s)FrequencyClinical significance
(Last reviewed)
Review status
1.
GRCh37:
ChrX:49047967
GRCh38:
ChrX:49191510
SYPnot specifiedLikely benign
(Jul 18, 2013)
criteria provided, single submitter
2.
GRCh37:
ChrX:49056641
GRCh38:
ChrX:49200182
SYP, SYP-AS1not specifiedGO-ESP:0.00028(T)Uncertain significance
(Jun 6, 2014)
criteria provided, single submitter
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