List of variants in gene TYROBP reported as benign for bone disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_003332.4(TYROBP):c.*25A>C	rs1802029	0.07474
NM_003332.4(TYROBP):c.*83C>T	rs14715	0.01070
NM_003332.4(TYROBP):c.163G>T (p.Val55Leu)	rs77782321	0.00810
NM_003332.4(TYROBP):c.94+10G>C	rs55746266	0.00630
NM_003332.4(TYROBP):c.*140T>C	rs113207157	0.00500
NM_003332.4(TYROBP):c.68G>A (p.Arg23His)	rs79272253	0.00061
NM_003332.4(TYROBP):c.123C>G (p.Gly41=)	rs111477177

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