ClinVar Miner

List of variants in gene HTRA1 studied for CARASIL syndrome; Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_002775.5(HTRA1):c.451C>A (p.Gln151Lys)	rs754645487	0.00019
NM_002775.5(HTRA1):c.33_34insTC (p.Leu12fs)
NM_002775.5(HTRA1):c.35dup (p.Leu13fs)
NM_002775.5(HTRA1):c.941T>C (p.Met314Thr)

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