List of variants in gene BLM reported as benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000057.4(BLM):c.2603C>T (p.Pro868Leu)	rs2227935	0.06742
NM_000057.4(BLM):c.419A>G (p.Glu140Gly)	rs35886055	0.00958
NM_000057.4(BLM):c.3960C>T (p.Pro1320=)	rs56009845	0.00502
NM_000057.4(BLM):c.615G>A (p.Lys205=)	rs28903082	0.00496
NM_000057.4(BLM):c.4076+4T>G	rs183176301	0.00436
NM_000057.4(BLM):c.410A>G (p.Lys137Arg)	rs28384988	0.00434
NM_000057.4(BLM):c.3128C>A (p.Ala1043Asp)	rs2229035	0.00421
NM_000057.4(BLM):c.1122T>C (p.His374=)	rs28385009	0.00382
NM_000057.4(BLM):c.1722A>G (p.Leu574=)	rs28385011	0.00379
NM_000057.4(BLM):c.893C>T (p.Thr298Met)	rs28384991	0.00346
NM_000057.4(BLM):c.1928G>A (p.Arg643His)	rs12720097	0.00278
NM_000057.4(BLM):c.4077-10C>T	rs145310008	0.00233

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