Related gene-specific medical variations for Gene (Select 101927863) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1292099	NC_000016.10:g.89508277G>C	LOC101927863, LOC130059818 +1 more	Single nucleotide variant	not provided	GBenign
Select item 1228084	NC_000016.10:g.89508194dup	LOC101927863, LOC130059818 +1 more	Duplication	not provided	GBenign
Select item 1209194	NC_000016.10:g.89508295A>C	LOC101927863, LOC130059818 +1 more	Single nucleotide variant	not provided	GLikely benign
Select item 1202937	NC_000016.10:g.89508278G>C	LOC101927863, LOC130059818 +1 more	Single nucleotide variant	not provided	GLikely benign

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