Related gene-specific medical variations for Gene (Select 346528) - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3302620	NM_001005287.2(OR2A1):c.202G>C (p.Val68Leu)	OR2A1, OR2A1-AS1 (V68L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204982	NM_001005287.2(OR2A1):c.330A>C (p.Glu110Asp)	OR2A1, OR2A1-AS1 (E110D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204981	NM_001005287.2(OR2A1):c.293C>T (p.Thr98Met)	OR2A1, OR2A1-AS1 (T98M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2658125	NM_001005287.2(OR2A1):c.40C>T (p.Leu14=)	OR2A1, OR2A1-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2560661	NM_001005287.2(OR2A1):c.257A>T (p.His86Leu)	OR2A1, OR2A1-AS1 (H86L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412325	NM_001005287.2(OR2A1):c.164A>C (p.His55Pro)	OR2A1, OR2A1-AS1 (H55P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381361	NM_001005287.2(OR2A1):c.305T>C (p.Leu102Pro)	OR2A1, OR2A1-AS1 (L102P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365770	NM_001005287.2(OR2A1):c.139C>G (p.Leu47Val)	OR2A1, OR2A1-AS1 (L47V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324607	NM_001005287.2(OR2A1):c.110C>A (p.Thr37Asn)	OR2A1, OR2A1-AS1 (T37N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296106	NM_001005287.2(OR2A1):c.166A>C (p.Thr56Pro)	OR2A1, OR2A1-AS1 (T56P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289300	NM_001005287.2(OR2A1):c.17C>G (p.Thr6Arg)	OR2A1, OR2A1-AS1 (T6R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261855	NM_001005287.2(OR2A1):c.55G>A (p.Gly19Ser)	OR2A1, OR2A1-AS1 (G19S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212626	NM_001005287.2(OR2A1):c.397G>A (p.Val133Ile)	OR2A1, OR2A1-AS1 (V133I)	Single nucleotide variant (missense variant)	not specified	GLikely benign