ClinVar Miner

List of variants in gene combination BRCA1, LOC126862571 reported as likely benign by Center for Precision Medicine, Meizhou People's Hospital

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.3739G>A (p.Val1247Ile)	rs80357191	0.00009
NM_007294.4(BRCA1):c.3596C>T (p.Ala1199Val)	rs587782458	0.00001

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