"PreventionGenetics, part of Exact Sciences"[submitter] AND "NR1I3"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3045625	NM_032174.6(TOMM40L):c.*695C>A	NR1I3, TOMM40L	Single nucleotide variant (3 prime UTR variant +1 more)	TOMM40L-related disorder	GLikely benign
Select item 197772	NM_005122.5(NR1I3):c.540C>T (p.Pro180=)	NR1I3	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 3058262	NM_005122.5(NR1I3):c.351C>T (p.Leu117=)	NR1I3	Single nucleotide variant (synonymous variant)	NR1I3-related disorder	GLikely benign
Select item 283162	NM_005122.5(NR1I3):c.289C>T (p.Arg97Trp)	NR1I3 (R97W +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign/Likely benign
Select item 3048641	NM_005122.5(NR1I3):c.144C>G (p.Pro48=)	NR1I3	Single nucleotide variant (synonymous variant)	NR1I3-related disorder	GLikely benign
Select item 3037402	NM_005122.5(NR1I3):c.-43A>G	NR1I3 (K4R)	Single nucleotide variant (5 prime UTR variant +1 more)	NR1I3-related disorder	GLikely benign

ClinVar