Related gene-specific medical variations for Gene (Select 84243) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3192680	NM_032283.3(ZDHHC18):c.127C>T (p.Pro43Ser)	LOC129929844, ZDHHC18 (P43S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612298	NM_032283.3(ZDHHC18):c.41C>T (p.Ala14Val)	LOC129929844, ZDHHC18 (A14V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313744	NM_032283.3(ZDHHC18):c.101G>A (p.Gly34Asp)	LOC129929844, ZDHHC18 (G34D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246240	NM_032283.3(ZDHHC18):c.122C>T (p.Ala41Val)	LOC129929844, ZDHHC18 (A41V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236338	NM_032283.3(ZDHHC18):c.142T>G (p.Trp48Gly)	LOC129929844, ZDHHC18 (W48G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231686	NM_032283.3(ZDHHC18):c.148A>C (p.Ser50Arg)	LOC129929844, ZDHHC18 (S50R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231685	NM_032283.3(ZDHHC18):c.145A>G (p.Ser49Gly)	LOC129929844, ZDHHC18 (S49G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229698	NM_032283.3(ZDHHC18):c.130G>C (p.Ala44Pro)	LOC129929844, ZDHHC18 (A44P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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