List of variants in gene KCNJ2 reported as not provided for Andersen Tawil syndrome

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000891.3(KCNJ2):c.953A>G (p.Asn318Ser)	rs367560052	0.00001
NM_000891.3(KCNJ2):c.199C>T (p.Arg67Trp)	rs104894580
NM_000891.3(KCNJ2):c.271_282del (p.Ala91_Leu94del)	rs797044841
NM_000891.3(KCNJ2):c.652C>T (p.Arg218Trp)	rs104894578
NM_000891.3(KCNJ2):c.665T>C (p.Leu222Ser)	rs1555603968
NM_000891.3(KCNJ2):c.899G>A (p.Gly300Asp)	rs104894579
NM_000891.3(KCNJ2):c.966G>C (p.Trp322Cys)	rs797044842

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