ClinVar Miner

List of variants in gene CLCN5 reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (962):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 31
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HGVS dbSNP
NM_001127898.4(CLCN5):c.*1447T>G rs543285083
NM_001127898.4(CLCN5):c.*1735T>C rs782712129
NM_001127898.4(CLCN5):c.*2860T>C rs140913229
NM_001127898.4(CLCN5):c.*3255C>T rs112868450
NM_001127898.4(CLCN5):c.*3409A>G rs59126550
NM_001127898.4(CLCN5):c.*3652T>C rs56657044
NM_001127898.4(CLCN5):c.*4192C>T rs148902882
NM_001127898.4(CLCN5):c.*4692C>T rs143625654
NM_001127898.4(CLCN5):c.*5140A>G rs182121138
NM_001127898.4(CLCN5):c.*5144C>T rs111560086
NM_001127898.4(CLCN5):c.*559A>G rs375542213
NM_001127898.4(CLCN5):c.*5956T>C rs932286
NM_001127898.4(CLCN5):c.*6372T>C rs573740499
NM_001127898.4(CLCN5):c.*6538G>A rs781863818
NM_001127898.4(CLCN5):c.*6955C>G
NM_001127898.4(CLCN5):c.1203G>C (p.Leu401=) rs34122840
NM_001127898.4(CLCN5):c.1223G>A (p.Arg408His)
NM_001127898.4(CLCN5):c.1243C>T (p.Arg415Trp) rs782817681
NM_001127898.4(CLCN5):c.1422G>A (p.Glu474=) rs199594074
NM_001127898.4(CLCN5):c.1473C>T (p.Gly491=) rs145670120
NM_001127898.4(CLCN5):c.1488T>C (p.Ser496=)
NM_001127898.4(CLCN5):c.1558-14G>C rs7063765
NM_001127898.4(CLCN5):c.1816G>A (p.Val606Met) rs782060809
NM_001127898.4(CLCN5):c.1914C>T (p.Pro638=) rs34173954
NM_001127898.4(CLCN5):c.315+12G>A
NM_001127898.4(CLCN5):c.416-6A>T rs6651602
NM_001127898.4(CLCN5):c.554A>G (p.Lys185Arg)
NM_001127898.4(CLCN5):c.636G>A (p.Met212Ile) rs34800648
NM_001127898.4(CLCN5):c.819= (p.Ser273=) rs34464675
NM_001127898.4(CLCN5):c.925C>T (p.Arg309Cys) rs782056386
NM_001127898.4(CLCN5):c.942G>A (p.Ser314=)

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