Related gene-specific medical variations for Gene (Select 5662) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2404678	NM_002779.5(PSD):c.2713C>T (p.Arg905Trp)	LOC124416894, PSD (R905W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2391830	NM_002779.5(PSD):c.2770G>A (p.Ala924Thr)	LOC124416894, PSD (A545T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2312631	NM_002779.5(PSD):c.2789G>A (p.Gly930Asp)	LOC124416894, PSD (G930D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2248598	NM_002779.5(PSD):c.2713C>G (p.Arg905Gly)	LOC124416894, PSD (R526G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 770767	NM_002779.5(PSD):c.2714G>A (p.Arg905Gln)	LOC124416894, PSD (R905Q +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 769787	NM_002779.5(PSD):c.2701-5G>A	LOC124416894, PSD	Single nucleotide variant (intron variant)	not provided	GLikely benign

ClinVar