ClinVar Miner

List of variants in gene NHS reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_001291867.2(NHS):c.3374C>T (p.Ser1125Leu) rs145005596 0.00053
NM_001291867.2(NHS):c.1163C>T (p.Ser388Leu) rs150689121 0.00009
NM_001291867.2(NHS):c.2047G>A (p.Val683Met) rs587780403 0.00003
NM_001291867.2(NHS):c.4813C>T (p.Arg1605Trp) rs370208884 0.00002
NM_001291867.2(NHS):c.503A>G (p.Gln168Arg) rs769860109 0.00002
NM_001291867.2(NHS):c.1415T>C (p.Ile472Thr) rs751213969 0.00001
NM_001291867.2(NHS):c.3262C>A (p.His1088Asn) rs924426347 0.00001
NM_001291867.2(NHS):c.176_177delinsAA (p.Arg59Gln) rs797045739
NM_001291867.2(NHS):c.1943_1945dup (p.Thr648dup) rs797045740
NM_001291867.2(NHS):c.333GGC[3] (p.Ala115_Ala117del) rs587780401
NM_001291867.2(NHS):c.333GGC[5] (p.Ala117del) rs587780401

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