List of variants in gene combination LFNG, LOC129997823 reported as uncertain significance for bone disorder

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001040167.2(LFNG):c.37C>G (p.Leu13Val)	rs1425455790	0.00006
NM_001040167.2(LFNG):c.46G>A (p.Ala16Thr)	rs1779735531	0.00001
NM_001040167.2(LFNG):c.10C>G (p.Arg4Gly)	rs1341252096
NM_001040167.2(LFNG):c.10C>T (p.Arg4Cys)	rs1341252096
NM_001040167.2(LFNG):c.41C>G (p.Ala14Gly)	rs1779735169
NM_001040167.2(LFNG):c.67G>T (p.Val23Leu)	rs2128375068

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