List of variants in gene combination ABCC2, LOC126861012 reported as benign for bilirubin metabolism disease

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000392.5(ABCC2):c.2883+11C>T	rs41318031	0.04549
NM_000392.5(ABCC2):c.2761G>A (p.Gly921Ser)	rs41318029	0.00860

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