Related gene-specific medical variations for Gene (Select 6623) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3295367	NM_024756.3(MMRN2):c.122G>C (p.Trp41Ser)	MMRN2, SNCG (W41S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2605333	NM_024756.3(MMRN2):c.163C>G (p.Arg55Gly)	MMRN2, SNCG (R55G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2539712	NM_024756.3(MMRN2):c.163C>T (p.Arg55Cys)	MMRN2, SNCG (R55C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2483450	NM_024756.3(MMRN2):c.62G>C (p.Trp21Ser)	MMRN2, SNCG (W21S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2243507	NM_024756.3(MMRN2):c.80C>G (p.Thr27Ser)	MMRN2, SNCG (T27S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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