Variants with conflicting interpretations "benign" from OMIM and "drug response" from any submitter

Minimum review status of the submission from OMIM:		Collection method of the submission from OMIM:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 3

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HGVS	dbSNP	gnomAD frequency
NM_001348946.2(ABCB1):c.3435T>C (p.Ile1145=)	rs1045642	0.57896
NM_000754.4(COMT):c.472G>A (p.Val158Met)	rs4680	0.44044
NM_005957.5(MTHFR):c.665C>T (p.Ala222Val)	rs1801133	0.27446

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