List of variants in gene MAN2B1 reported as benign for not specified

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

Total variants: 8

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HGVS	dbSNP
NM_000528.4(MAN2B1):c.1010G>A (p.Arg337Gln)	rs1133330
NM_000528.4(MAN2B1):c.1068C>G (p.Pro356=)	rs117880912
NM_000528.4(MAN2B1):c.1238A>G (p.Asn413Ser)	rs35836657
NM_000528.4(MAN2B1):c.1441G>T (p.Ala481Ser)	rs34544747
NM_000528.4(MAN2B1):c.2006C>T (p.Pro669Leu)	rs75029862
NM_000528.4(MAN2B1):c.747C>T (p.Thr249=)	rs61737536
NM_000528.4(MAN2B1):c.832C>G (p.Leu278Val)	rs1054486
NM_000528.4(MAN2B1):c.935C>T (p.Thr312Ile)	rs1054487

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