"Illumina Laboratory Services, Illumina"[submitter] AND "LOC109611593" - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 357085	NM_003599.4(SUPT3H):c.101+36794A>G	LOC109611593, RUNX2 +1 more	Single nucleotide variant (5 prime UTR variant +2 more)	Cleidocranial dysostosis	GBenign
Select item 357086	NM_003599.4(SUPT3H):c.101+36554C>A	LOC109611593, RUNX2 +1 more	Single nucleotide variant (intron variant)	Cleidocranial dysostosis	GBenign