List of variants in gene combination FANCD2, LOC107303338 reported as benign for female reproductive system neoplasm

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001018115.3(FANCD2):c.1156T>G (p.Phe386Val)	rs149125003	0.00450
NM_001018115.3(FANCD2):c.2068G>A (p.Asp690Asn)	rs534038231	0.00005

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