Related gene-specific medical variations for Gene (Select 1039) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3141703	NM_001802.2(CDR2):c.49C>T (p.Pro17Ser)	CDR2, LOC130058644 (P17S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2646314	NM_001802.2(CDR2):c.18G>A (p.Leu6=)	CDR2, LOC130058644	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2549514	NM_001802.2(CDR2):c.58G>A (p.Asp20Asn)	CDR2, LOC130058644 (D20N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361334	NM_001802.2(CDR2):c.65A>G (p.Gln22Arg)	CDR2, LOC130058644 (Q22R)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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