Related gene-specific medical variations for Gene (Select 5986) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3313871	NM_002917.2(RFNG):c.178G>A (p.Val60Ile)	GPS1, RFNG (V60I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3313870	NM_002917.2(RFNG):c.155C>T (p.Ala52Val)	GPS1, RFNG (A52V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3313869	NM_002917.2(RFNG):c.166C>T (p.Arg56Trp)	GPS1, RFNG (R56W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2648483	NM_002917.2(RFNG):c.6C>T (p.Ser2=)	GPS1, RFNG	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2517688	NM_002917.2(RFNG):c.167G>A (p.Arg56Gln)	GPS1, RFNG (R56Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2345671	NM_002917.2(RFNG):c.202C>T (p.Arg68Trp)	GPS1, RFNG (R68W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2342657	NM_002917.2(RFNG):c.215G>C (p.Gly72Ala)	GPS1, RFNG (G72A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 716492	NM_002917.2(RFNG):c.201C>T (p.Thr67=)	GPS1, RFNG	Single nucleotide variant (synonymous variant)	not provided	GBenign

ClinVar