"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "GRSF1"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2654798	NM_002092.4(GRSF1):c.1104C>T (p.Pro368=)	GRSF1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2654799	NM_002092.4(GRSF1):c.-1C>T	GRSF1	Single nucleotide variant (5 prime UTR variant)	not provided	GLikely benign
Select item 3024631	GRCh37/hg19 4p12-q35.2(chr4:45455621-191003541)x3	TMA16, CXCL1 +537 more	Copy number gain	not provided	GPathogenic

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