List of variants in gene BTK reported as likely benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000061.3(BTK):c.1178-207C>T	rs60771146	0.01444
NM_000061.3(BTK):c.-30-162C>A	rs3027625	0.00707
NM_000061.3(BTK):c.615G>T (p.Glu205Asp)	rs35877704	0.00114
NM_000061.3(BTK):c.1701A>G (p.Glu567=)	rs146681416	0.00032
NM_000061.3(BTK):c.1164A>G (p.Ala388=)	rs1603005571
NM_000061.3(BTK):c.1746T>C (p.Ala582=)	rs1603002337
NM_000061.3(BTK):c.1908+294del	rs60191867
NM_000061.3(BTK):c.1909-134del	rs199950200
NM_000061.3(BTK):c.391+165_391+168del	rs200888149
NM_000061.3(BTK):c.520+15C>T	rs782697907

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