List of variants in gene LFNG reported as benign for autosomal recessive disease

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001040167.2(LFNG):c.482-4A>G	rs62444250	0.05791
NM_001040167.2(LFNG):c.972G>A (p.Ser324=)	rs12700028	0.04179
NM_001040167.2(LFNG):c.1002C>T (p.Tyr334=)	rs61743870	0.03693
NM_001040167.2(LFNG):c.481+3G>A	rs141008352	0.00361
NM_001040167.2(LFNG):c.612C>T (p.Tyr204=)	rs147266260	0.00105
NM_001040167.2(LFNG):c.581+14C>T	rs371327031	0.00061
NM_001040167.2(LFNG):c.920G>A (p.Arg307His)	rs201791522	0.00021
NM_001040167.2(LFNG):c.988-12C>T	rs200232463	0.00019
NM_001040167.2(LFNG):c.822-9C>G	rs199661195	0.00017
NM_001040167.2(LFNG):c.988-16C>T	rs376736772	0.00002
NM_001040167.2(LFNG):c.1104G>A (p.Pro368=)	rs544123371

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