ClinVar Miner

List of variants reported as likely benign by Institute of Reproductive Genetics, University of Münster

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Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_001350162.2(TEX15):c.7118G>A (p.Ser2373Asn) rs61738844 0.01620
NM_000492.4(CFTR):c.2245C>T (p.Leu749=) rs151235408 0.00056
NM_001039111.3(TRIM71):c.553G>T (p.Ala185Ser) rs781320370 0.00053
NM_001039111.3(TRIM71):c.785G>C (p.Gly262Ala) rs769421964 0.00002
NM_014940.4(MON1B):c.*1165C>G rs112674196

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