List of variants in gene combination LOC130009662, TNFSF11 reported as benign for autosomal recessive osteopetrosis 2

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_003701.4(TNFSF11):c.-127C>G	rs9533157	0.99807
NM_003701.4(TNFSF11):c.126T>C (p.Pro42=)	rs2296533	0.47237
NM_003701.4(TNFSF11):c.147C>T (p.Phe49=)	rs61735535	0.00938
NM_003701.4(TNFSF11):c.80A>G (p.Glu27Gly)	rs200788562	0.00262

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