ClinVar Miner

List of variants reported as uncertain significance for Neuropathy, hereditary sensory and autonomic, type 2A by Genomic Research Center, Shahid Beheshti University of Medical Sciences

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001365536.1(SCN9A):c.3767A>G (p.Asn1256Ser)	rs141268327	0.00496
NM_018979.4(WNK1):c.5068C>G (p.Pro1690Ala)	rs771546256	0.00003
NM_018979.4(WNK1):c.2187G>A (p.Gly729=)	rs759764709

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