"Illumina Laboratory Services, Illumina"[submitter] AND "LOC130000232" - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 911062	NM_023110.3(FGFR1):c.-116C>T	FGFR1, LOC130000232	Single nucleotide variant (5 prime UTR variant)	Craniosynostosis syndrome +3 more	GUncertain significance
Select item 911063	NM_023110.3(FGFR1):c.-117C>G	FGFR1, LOC130000232	Single nucleotide variant (5 prime UTR variant)	Craniosynostosis syndrome +3 more	GUncertain significance
Select item 362912	NM_023110.3(FGFR1):c.-124G>A	FGFR1, LOC130000232	Single nucleotide variant (5 prime UTR variant)	Osteoglophonic dysplasia +3 more	GBenign

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ClinVar