List of variants in gene TYROBP studied for bone disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 24

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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.-34C>T	rs199931680	0.00152
NM_003332.4(TYROBP):c.46C>T (p.Leu16=)	rs147393700	0.00121
NM_003332.4(TYROBP):c.*85C>T	rs374144427	0.00071
NM_003332.4(TYROBP):c.68G>A (p.Arg23His)	rs79272253	0.00061
NM_003332.4(TYROBP):c.*103T>A	rs777094340	0.00032
NM_003332.4(TYROBP):c.-50G>A	rs371441146	0.00008
NM_003332.4(TYROBP):c.140T>C (p.Val47Ala)	rs372140827	0.00006
NM_003332.4(TYROBP):c.*5G>A	rs372703196	0.00004
NM_003332.4(TYROBP):c.111G>A (p.Thr37=)	rs200694727	0.00004
NM_003332.4(TYROBP):c.*154T>C	rs554715202	0.00003
NM_003332.4(TYROBP):c.112G>A (p.Val38Met)	rs199970556	0.00001
NM_003332.4(TYROBP):c.141del (p.Met48fs)	rs386833840	0.00001
NM_003332.4(TYROBP):c.180C>G (p.Ala60=)	rs199583341	0.00001
NM_003332.4(TYROBP):c.230-3C>T	rs779491857	0.00001
NM_003332.4(TYROBP):c.116G>A (p.Ser39Asn)	rs386833839
NM_003332.4(TYROBP):c.123C>G (p.Gly41=)	rs111477177
NM_003332.4(TYROBP):c.145G>C (p.Gly49Arg)	rs386833841
NM_003332.4(TYROBP):c.262G>T (p.Glu88Ter)	rs386833842
NM_003332.4(TYROBP):c.2T>C (p.Met1Thr)	rs104894732

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