Related gene-specific medical variations for Gene (Select 9260) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3211020	NM_005451.5(PDLIM7):c.418G>C (p.Val140Leu)	LOC121099718, PDLIM7 (V106L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2359577	NM_005451.5(PDLIM7):c.542A>G (p.Asp181Gly)	LOC121099718, PDLIM7 (D181G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2306802	NM_005451.5(PDLIM7):c.470C>T (p.Pro157Leu)	LOC121099718, PDLIM7 (P123L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2302608	NM_005451.5(PDLIM7):c.418G>A (p.Val140Ile)	LOC121099718, PDLIM7 (V140I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2294812	NM_005451.5(PDLIM7):c.473G>A (p.Arg158Gln)	LOC121099718, PDLIM7 (R124Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 733996	NM_005451.5(PDLIM7):c.536-8C>T	LOC121099718, PDLIM7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 727280	NM_005451.5(PDLIM7):c.477G>A (p.Pro159=)	LOC121099718, PDLIM7	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign

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