ClinVar Miner

List of variants in gene CTSD reported as benign for not provided

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Gene type:
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Total variants: 11
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HGVS dbSNP
NC_000011.10:g.1764171T>C rs144932926
NM_001909.5(CTSD):c.1072-34T>C rs112379600
NM_001909.5(CTSD):c.173C>T (p.Ala58Val) rs17571
NM_001909.5(CTSD):c.189C>T (p.Thr63=) rs114051835
NM_001909.5(CTSD):c.231C>T (p.Ala77=) rs2230067
NM_001909.5(CTSD):c.353-17C>T rs7126177
NM_001909.5(CTSD):c.465T>C (p.Thr155=) rs11555039
NM_001909.5(CTSD):c.472-161G>T rs60582924
NM_001909.5(CTSD):c.704+233G>A rs2292962
NM_001909.5(CTSD):c.705-74C>T rs2292963
NM_001909.5(CTSD):c.828-17G>A rs78735768

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