Related gene-specific medical variations for Gene (Select 4018) - ClinVar - NCBI

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Links from Gene

Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3291134	NM_005577.4(LPA):c.2804C>T (p.Pro935Leu)	LOC126859860, LPA (P935L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119668	NM_005577.4(LPA):c.2827G>A (p.Gly943Arg)	LOC126859860, LPA (G943R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2657113	NM_005577.4(LPA):c.2804C>G (p.Pro935Arg)	LOC126859860, LPA (P935R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1706478	LPA +121A	LPA	Single nucleotide variant	Not Specified	Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant
Select item 1706477	LPA +93C	LPA	Single nucleotide variant	Not Specified	Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant
Select item 1706476	LPA -773A	LPA	Single nucleotide variant	Not Specified	Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant
Select item 988870	NM_005577.4(LPA):c.5081C>G (p.Ser1694Ter)	LPA (S1694*)	Single nucleotide variant (nonsense)	Abnormal bleeding +1 more	GUncertain significance
Select item 975029	G4925A	LPA	Single nucleotide variant	LIPOPROTEIN(a) POLYMORPHISM	GBenign
Select item 14447	Multiple alleles	LPA	Single nucleotide variant	APOLIPOPROTEIN(a), TYPE C POLYMORPHISM	GBenign