List of variants in gene combination LRRC14, LRRC24 reported as likely benign by Ambry Genetics

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)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001024678.4(LRRC24):c.29C>T (p.Pro10Leu)	rs772340139	0.00001
NM_001024678.4(LRRC24):c.407G>A (p.Arg136Gln)	rs755474129	0.00001
NM_001024678.4(LRRC24):c.10A>G (p.Arg4Gly)
NM_001024678.4(LRRC24):c.889C>G (p.Pro297Ala)

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