ClinVar Miner

List of variants in gene DYSF reported as likely benign by CeGaT Praxis fuer Humangenetik Tuebingen

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Gene type:
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Total variants: 8
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HGVS dbSNP
NM_001130987.2(DYSF):c.1216G>C (p.Val406Leu) rs150724610
NM_001130987.2(DYSF):c.1299C>T (p.Asn433=) rs757047049
NM_001130987.2(DYSF):c.3111C>T (p.Pro1037=) rs143475751
NM_001130987.2(DYSF):c.3946A>G (p.Ile1316Val) rs121908954
NM_001130987.2(DYSF):c.4037C>T (p.Ala1346Val) rs201476613
NM_001130987.2(DYSF):c.4261G>A (p.Val1421Ile) rs767049254
NM_001130987.2(DYSF):c.45G>A (p.Ala15=) rs972675695
NM_001130987.2(DYSF):c.5743G>A (p.Asp1915Asn) rs115013641

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