"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "MFSD11"[ge - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2648320	NM_001195427.2(SRSF2):c.183C>T (p.Arg61=)	MFSD11, SRSF2	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 1701331	GRCh37/hg19 17q25.1-25.3(chr17:73481509-81043199)x3	SLC26A11, SLC38A10 +146 more	Copy number gain	not provided	GPathogenic
Select item 624519	GRCh37/hg19 17q24.1-25.2(chr17:64159738-74891024)x3	LLGL2, MAP2K6 +119 more	Copy number gain	not provided	GLikely pathogenic

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