ClinVar Miner

List of variants in gene NSMF reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_001130969.3(NSMF):c.704+191A>G rs551266961 0.01223
NM_001130969.3(NSMF):c.704+114A>C rs73669104 0.01153
NM_001130969.3(NSMF):c.71+178C>G rs35043345 0.01136
NM_001130969.3(NSMF):c.705-168G>A rs79745041 0.01076
NM_001130969.3(NSMF):c.833-217T>A rs183070606 0.00987
NM_001130969.3(NSMF):c.704+119C>T rs74861169 0.00763
NM_001130969.3(NSMF):c.1047+58C>T rs114999343 0.00524
NM_001130969.3(NSMF):c.779+245C>T rs77778636 0.00519
NM_001130969.3(NSMF):c.134-17C>T rs149347630 0.00364
NM_001130969.3(NSMF):c.704+202_704+203insA rs59030620
NM_001130969.3(NSMF):c.704+203CA[5] rs201928724

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