Related gene-specific medical variations for Gene (Select 54847) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3318444	NM_017699.3(SIDT1):c.127G>T (p.Ala43Ser)	LOC129937254, SIDT1 (A43S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3162068	NM_017699.3(SIDT1):c.127G>A (p.Ala43Thr)	LOC129937254, SIDT1 (A43T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance