ClinVar for MedGen (Select 65117) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 830363	NM_000183.3(HADHB):c.110-2324G>C	HADHB (W12C)	Single nucleotide variant (intron variant +1 more)	Renal tubular acidosis +2 more	GUncertain significance
Select item 694733	NM_001128831.4(CA1):c.368_369del (p.His123fs)	CA1 (H10fs +2 more)	Deletion (frameshift variant)	Renal tubular acidosis +2 more	GUncertain significance