Related gene-specific medical variations for Gene (Select 116028) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3314621	NM_152308.3(RMI2):c.293C>G (p.Pro98Arg)	LOC130058493, RMI2 (P98R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2685556	GRCh37/hg19 16p13.13(chr16:11431847-11517285)x1	RMI2	Copy number loss	not provided	GUncertain significance
Select item 2539893	NM_152308.3(RMI2):c.274G>T (p.Gly92Trp)	LOC130058493, RMI2 (G92W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490611	NM_152308.3(RMI2):c.263G>A (p.Arg88Gln)	LOC130058493, RMI2 (R88Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405821	NM_152308.3(RMI2):c.61C>A (p.Pro21Thr)	LOC130058492, RMI2 (P21T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2382533	NM_152308.3(RMI2):c.109G>T (p.Gly37Cys)	LOC130058492, RMI2 (G37C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303870	NM_152308.3(RMI2):c.170C>T (p.Ala57Val)	LOC130058492, RMI2 (A57V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 564272	GRCh37/hg19 16p13.13(chr16:11387163-11489720)x1	RMI2	Copy number loss	not provided	GUncertain significance
Select item 135275	NM_003745.2(SOCS1):c.630G>C (p.Gln210His)	RMI2, SOCS1 (Q210H)	Single nucleotide variant (missense variant)	not provided	GLikely benign

ClinVar