List of variants in gene BLK reported as benign by PreventionGenetics, part of Exact Sciences

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001715.3(BLK):c.843T>C (p.Phe281=)	rs2306234	0.81190
NM_001715.3(BLK):c.330T>C (p.Ser110=)	rs3816668	0.49161
NC_000008.11:g.11573132C>T	rs61199332	0.06287
NM_001715.3(BLK):c.258G>A (p.Gln86=)	rs56185487	0.02041
NM_001715.3(BLK):c.211G>A (p.Ala71Thr)	rs55758736	0.01485
NM_001715.3(BLK):c.102C>T (p.Asp34=)	rs75383960	0.00743
NM_001715.3(BLK):c.711C>T (p.Pro237=)	rs143699141	0.00174
NM_001715.3(BLK):c.39G>A (p.Lys13=)	rs142129056

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