ClinVar Miner

List of variants in gene MAN2B1 reported as benign by GeneDx

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Gene type:
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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_000528.4(MAN2B1):c.2046+184A>G rs17476839 0.66859
NM_000528.4(MAN2B1):c.2267+63A>G rs3815914 0.66212
NM_000528.4(MAN2B1):c.2267+216A>G rs8102193 0.59793
NM_000528.4(MAN2B1):c.1310-22C>T rs73002392 0.50963
NM_000528.4(MAN2B1):c.1026+251T>C rs8108316 0.42644
NM_000528.4(MAN2B1):c.910-73A>G rs2303731 0.40412
NM_000528.4(MAN2B1):c.1010G>A (p.Arg337Gln) rs1133330 0.34583
NM_000528.4(MAN2B1):c.832C>G (p.Leu278Val) rs1054486 0.30800
NM_000528.4(MAN2B1):c.631-213C>T rs8104821 0.28087
NM_000528.4(MAN2B1):c.1309+34C>A rs34324185 0.27121
NM_000528.4(MAN2B1):c.1238A>G (p.Asn413Ser) rs35836657 0.08930
NM_000528.4(MAN2B1):c.2924-152G>A rs61161691 0.08170
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.2046+194A>G rs73002389 0.04623
NM_000528.4(MAN2B1):c.1420-40G>C rs112072150 0.02633
NM_000528.4(MAN2B1):c.2310C>T (p.Pro770=) rs35880640 0.02554
NM_000528.4(MAN2B1):c.1310-56C>T rs77179562 0.02241
NM_000528.4(MAN2B1):c.1026+261A>G rs10422318 0.02170
NM_000528.4(MAN2B1):c.910-174G>T rs79674546 0.02077
NM_000528.4(MAN2B1):c.2267+3G>C rs28639634 0.02031
NM_000528.4(MAN2B1):c.2221G>A (p.Gly741Arg) rs61234887 0.01841
NM_000528.4(MAN2B1):c.2436+243C>T rs142932540 0.01689
NM_000528.4(MAN2B1):c.1068C>G (p.Pro356=) rs117880912 0.00217
NM_000528.4(MAN2B1):c.1644+199dup rs372686781
NM_000528.4(MAN2B1):c.1830+138C>T rs8107642
NM_000528.4(MAN2B1):c.1831-158T>G rs4804205
NM_000528.4(MAN2B1):c.1831-89_1831-88dup rs71168621
NM_000528.4(MAN2B1):c.1831-89dup rs71168621
NM_000528.4(MAN2B1):c.2047-136del rs35532533
NM_000528.4(MAN2B1):c.2268-45T>G rs12984441
NM_000528.4(MAN2B1):c.909+82G>C rs79932579
NM_000528.4(MAN2B1):c.935C>T (p.Thr312Ile) rs1054487

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