ClinVar Miner

List of variants in gene WNK1 reported as likely pathogenic for Neuropathy, hereditary sensory and autonomic, type 2A

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_213655.5(WNK1):c.3633+1G>T	rs762015494	0.00003
NM_213655.5(WNK1):c.2229dup (p.Thr744fs)	rs1307515994

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