ClinVar Miner

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

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP
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.*5144C>T rs111560086
NM_001127898.4(CLCN5):c.*5956T>C rs932286
NM_001127898.4(CLCN5):c.1203G>C (p.Leu401=) rs34122840
NM_001127898.4(CLCN5):c.1558-14G>C rs7063765
NM_001127898.4(CLCN5):c.1914C>T (p.Pro638=) rs34173954
NM_001127898.4(CLCN5):c.416-6A>T rs6651602
NM_001127898.4(CLCN5):c.819= (p.Ser273=) rs34464675

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