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

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000528.4(MAN2B1):c.1010G>A (p.Arg337Gln)	rs1133330	0.33916
NM_000528.4(MAN2B1):c.832C>G (p.Leu278Val)	rs1054486	0.29947
NM_000528.4(MAN2B1):c.1238A>G (p.Asn413Ser)	rs35836657	0.08930
NM_000528.4(MAN2B1):c.1441G>T (p.Ala481Ser)	rs34544747	0.07202
NM_000528.4(MAN2B1):c.747C>T (p.Thr249=)	rs61737536	0.05436
NM_000528.4(MAN2B1):c.2562C>G (p.Ala854=)	rs10410289	0.00964
NM_000528.4(MAN2B1):c.2006C>T (p.Pro669Leu)	rs75029862	0.00451
NM_000528.4(MAN2B1):c.1581G>A (p.Arg527=)	rs149613968	0.00328
NM_000528.4(MAN2B1):c.1068C>G (p.Pro356=)	rs117880912	0.00217
NM_000528.4(MAN2B1):c.2865G>C (p.Thr955=)	rs148108322	0.00175
NM_000528.4(MAN2B1):c.1437G>T (p.Ala479=)	rs139435774	0.00045
NM_000528.4(MAN2B1):c.1158G>A (p.Gln386=)	rs112829030	0.00025
NM_000528.4(MAN2B1):c.1231-13C>T	rs372848519
NM_000528.4(MAN2B1):c.935C>A (p.Thr312Asn)	rs1054487
NM_000528.4(MAN2B1):c.935C>T (p.Thr312Ile)	rs1054487

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