List of variants in gene BTK reported as benign for not specified

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000061.3(BTK):c.1899C>T (p.Cys633=)	rs1135363	0.37760
NM_000061.3(BTK):c.141+11C>T	rs138411530	0.00620
NM_000061.3(BTK):c.1252T>C (p.Tyr418His)	rs144079566	0.00029
NM_000061.3(BTK):c.895-10G>A	rs370812397	0.00010
NM_000061.3(BTK):c.1350-29A>G
NM_000061.3(BTK):c.1631+71C>T	rs2071223
NM_000061.3(BTK):c.391+143dup	rs193922127

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