Related gene-specific medical variations for Gene (Select 100506054) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1246180	NC_000002.12:g.3558529A>G	LOC129933003, RNASEH1 +1 more	Single nucleotide variant (non-coding transcript variant)	not provided	GBenign
Select item 683667	NM_002936.4(RNASEH1):c.-128T>C	LOC129933002, RNASEH1 +1 more	Single nucleotide variant (non-coding transcript variant)	not provided	GLikely benign
Select item 673768	NM_002936.4(RNASEH1):c.-126A>G	RNASEH1-DT, LOC129933002 +1 more	Single nucleotide variant (non-coding transcript variant)	not provided	GBenign

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