"Illumina Laboratory Services, Illumina"[submitter] AND "LOC129992073" - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Format

Sort by

Choose Destination

Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 348618	NM_001122681.2(SH3BP2):c.*1655C>T	SH3BP2, LOC129992073	Single nucleotide variant (3 prime UTR variant)	Fibrous dysplasia of jaw	GLikely benign
Select item 348619	NM_001122681.2(SH3BP2):c.*1656T>C	LOC129992073, SH3BP2	Single nucleotide variant (3 prime UTR variant)	Fibrous dysplasia of jaw	GBenign
Select item 348620	NM_001122681.2(SH3BP2):c.*1679C>T	LOC129992073, SH3BP2	Single nucleotide variant (3 prime UTR variant)	Fibrous dysplasia of jaw	GBenign

Format

Sort by

Choose Destination