Related gene-specific medical variations for Gene (Select 6013) - ClinVar - NCBI

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Links from Gene

Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3314584	NM_006911.4(RLN1):c.239A>G (p.Asp80Gly)	RLN1, RLN2 (D80G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3314582	NM_006911.4(RLN1):c.290A>C (p.Glu97Ala)	RLN1, RLN2 (E97A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3154754	NM_006911.4(RLN1):c.463A>G (p.Thr155Ala)	RLN1, RLN2 (T155A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3154753	NM_006911.4(RLN1):c.416A>G (p.Glu139Gly)	RLN1, RLN2 (E139G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3154751	NM_006911.4(RLN1):c.255T>G (p.Ile85Met)	RLN1, RLN2 (I85M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511798	NM_006911.4(RLN1):c.401G>A (p.Arg134His)	RLN1, RLN2 (R134H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2486008	NM_006911.4(RLN1):c.526T>C (p.Cys176Arg)	RLN1, RLN2 (C176R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375309	NM_006911.4(RLN1):c.370C>G (p.Leu124Val)	RLN1, RLN2 (L124V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360732	NM_006911.4(RLN1):c.467A>C (p.His156Pro)	RLN1, RLN2 (H156P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 718077	NM_006911.4(RLN1):c.219A>C (p.Val73=)	RLN1, RLN2	Single nucleotide variant (synonymous variant)	not provided	GBenign