Related gene-specific medical variations for Gene (Select 100873939) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3291044	NM_001126328.3(LNX1):c.410C>G (p.Thr137Ser)	LNX1, LNX1-AS1 (T41S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119491	NM_001126328.3(LNX1):c.673A>T (p.Asn225Tyr)	LNX1, LNX1-AS1 (N129Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119490	NM_001126328.3(LNX1):c.646A>G (p.Ile216Val)	LNX1, LNX1-AS1 (I120V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119489	NM_001126328.3(LNX1):c.625C>T (p.Arg209Trp)	LNX1, LNX1-AS1 (R209W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617447	NM_001126328.3(LNX1):c.526G>A (p.Glu176Lys)	LNX1, LNX1-AS1 (E176K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356972	NM_001126328.3(LNX1):c.637A>G (p.Arg213Gly)	LNX1, LNX1-AS1 (R117G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317636	NM_001126328.3(LNX1):c.773A>G (p.Glu258Gly)	LNX1, LNX1-AS1 (E162G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215724	NM_001126328.3(LNX1):c.708C>G (p.Ser236Arg)	LNX1, LNX1-AS1 (S140R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar