Related gene-specific medical variations for Gene (Select 51312) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3319236	NM_016612.4(SLC25A37):c.162G>A (p.Met54Ile)	LOC130000035, SLC25A37 (M54I)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3163715	NM_016612.4(SLC25A37):c.124A>G (p.Ser42Gly)	LOC130000035, SLC25A37 (S42G)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2619266	NM_016612.4(SLC25A37):c.91A>T (p.Thr31Ser)	LOC130000035, SLC25A37 (T31S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2474053	NM_016612.4(SLC25A37):c.128C>G (p.Ala43Gly)	LOC130000035, SLC25A37 (A43G)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2293359	NM_016612.4(SLC25A37):c.125G>C (p.Ser42Thr)	LOC130000035, SLC25A37 (S42T)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2227021	NM_016612.4(SLC25A37):c.46A>G (p.Arg16Gly)	LOC130000035, SLC25A37 (R16G)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

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