"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC126861 - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3061583	NM_000392.5(ABCC2):c.2625T>C (p.His875=)	ABCC2, LOC126861012	Single nucleotide variant (synonymous variant)	ABCC2-related disorder	GLikely benign
Select item 3051603	NM_000392.5(ABCC2):c.2637A>G (p.Glu879=)	ABCC2, LOC126861012	Single nucleotide variant (synonymous variant)	ABCC2-related disorder	GLikely benign
Select item 3012617	NM_000392.5(ABCC2):c.2640A>G (p.Glu880=)	ABCC2, LOC126861012	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2893275	NM_000392.5(ABCC2):c.2649T>C (p.Asp883=)	ABCC2, LOC126861012	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 501698	NM_000392.5(ABCC2):c.2732G>A (p.Arg911Gln)	LOC126861012, ABCC2 (R911Q)	Single nucleotide variant (missense variant)	ABCC2-related disorder +1 more	GUncertain significance
Select item 282329	NM_000392.5(ABCC2):c.2743C>T (p.Arg915Cys)	LOC126861012, ABCC2 (R915C)	Single nucleotide variant (missense variant)	ABCC2-related disorder +3 more	GLikely benign
Select item 298459	NM_000392.5(ABCC2):c.2747+5G>A	ABCC2, LOC126861012	Single nucleotide variant (intron variant)	Dubin-Johnson syndrome +2 more	GBenign/Likely benign
Select item 3054632	NM_000392.5(ABCC2):c.2791T>C (p.Leu931=)	ABCC2, LOC126861012	Single nucleotide variant (synonymous variant)	ABCC2-related disorder	GLikely benign
Select item 282331	NM_000392.5(ABCC2):c.2813G>A (p.Ser938Asn)	ABCC2, LOC126861012 (S938N)	Single nucleotide variant (missense variant)	not specified +3 more	GLikely benign