List of variants in gene WNK1 reported as uncertain significance by Eurofins NTD LLC (GA)

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)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_018979.4(WNK1):c.1074C>T (p.Thr358=)	rs72648621	0.00160
NM_018979.4(WNK1):c.6150T>C (p.Leu2050=)	rs151331381	0.00157
NM_018979.4(WNK1):c.3578G>A (p.Ser1193Asn)	rs72650720	0.00045
NM_018979.4(WNK1):c.3210T>C (p.Ser1070=)	rs72650717	0.00008
NM_018979.4(WNK1):c.5734A>C (p.Ile1912Leu)	rs201995891	0.00006
NM_018979.4(WNK1):c.6278G>A (p.Arg2093His)	rs200315094	0.00006
NM_018979.4(WNK1):c.1769A>G (p.Lys590Arg)	rs780986326	0.00004
NM_018979.4(WNK1):c.3209+3A>G	rs886044182	0.00001
NM_018979.4(WNK1):c.2532T>A (p.Ile844=)	rs762491690
NM_018979.4(WNK1):c.2896G>A (p.Val966Met)	rs886042915
NM_018979.4(WNK1):c.46C>T (p.Leu16=)	rs1443431827
NM_018979.4(WNK1):c.5520C>T (p.Val1840=)	rs1212431255

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