ClinVar Miner

List of variants in gene CLCN1 reported as likely benign for not specified

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Gene type:
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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_000083.3(CLCN1):c.1065-16T>C rs113764654 0.00833
NM_000083.3(CLCN1):c.501C>G (p.Phe167Leu) rs149729531 0.00075
NM_000083.3(CLCN1):c.2541C>T (p.His847=) rs146653916 0.00027
NM_000083.3(CLCN1):c.900G>A (p.Arg300=) rs149578972 0.00022
NM_000083.3(CLCN1):c.1583-12G>A rs374736253 0.00019
NM_000083.3(CLCN1):c.1605C>T (p.Ala535=) rs200676193 0.00009
NM_000083.3(CLCN1):c.434-14A>G rs200263856 0.00009
NM_000083.3(CLCN1):c.2937C>T (p.Asp979=) rs776873546 0.00005
NM_000083.3(CLCN1):c.1593G>A (p.Ala531=) rs367696668 0.00004
NM_000083.3(CLCN1):c.13C>T (p.Arg5Trp) rs1322496244 0.00003
NM_000083.3(CLCN1):c.2847C>T (p.Gly949=) rs760793323 0.00003
NM_000083.3(CLCN1):c.2509-16T>G rs774042985 0.00002
NM_000083.3(CLCN1):c.655C>T (p.Leu219=) rs1427322271 0.00002
NM_000083.3(CLCN1):c.720C>T (p.Ser240=) rs764402957 0.00002
NM_000083.3(CLCN1):c.1863A>G (p.Thr621=) rs369099862 0.00001
NM_000083.3(CLCN1):c.2284+19G>A rs769666294 0.00001
NM_000083.3(CLCN1):c.1482T>C (p.Phe494=) rs745690349
NM_000083.3(CLCN1):c.153C>T (p.Gly51=) rs1554433799
NM_000083.3(CLCN1):c.2883G>C (p.Gly961=) rs1057522756
NM_000083.3(CLCN1):c.853+19C>A rs748877906
NM_000083.3(CLCN1):c.854-8C>T rs201115855

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