Related gene-specific medical variations for Gene (Select 119) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3269950	NM_001617.4(ADD2):c.1222G>A (p.Val408Met)	ADD2, LOC126806247 (V424M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082774	NM_001617.4(ADD2):c.1252G>C (p.Ala418Pro)	ADD2, LOC126806247 (A434P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082765	NM_001617.4(ADD2):c.1174A>T (p.Thr392Ser)	ADD2, LOC126806247 (T392S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082762	NM_001617.4(ADD2):c.1168G>A (p.Glu390Lys)	ADD2, LOC126806247 (E406K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389281	NM_001617.4(ADD2):c.1244C>T (p.Pro415Leu)	ADD2, LOC126806247 (P431L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274641	NM_001617.4(ADD2):c.1399G>A (p.Glu467Lys)	ADD2, LOC126806247 (E467K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264473	NM_001617.4(ADD2):c.1256T>G (p.Leu419Arg)	ADD2, LOC126806247 (L435R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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