List of variants in gene KCNJ2 reported as likely benign for not provided

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_000891.3(KCNJ2):c.*1596A>C	rs117409545	0.02347
NM_000891.3(KCNJ2):c.*1350G>A	rs116077770	0.00360
NM_000891.3(KCNJ2):c.-216-169G>C	rs75529334	0.00337
NM_000891.3(KCNJ2):c.1229A>G (p.Asn410Ser)	rs141069645	0.00042
NM_000891.3(KCNJ2):c.372C>T (p.Ser124=)	rs138877244	0.00024
NM_000891.3(KCNJ2):c.327C>T (p.Leu109=)	rs140274795	0.00009
NM_000891.3(KCNJ2):c.1080C>T (p.Asp360=)	rs66476803	0.00007
NM_000891.3(KCNJ2):c.1222C>G (p.Leu408Val)	rs753757610	0.00005
NM_000891.3(KCNJ2):c.597C>T (p.Ala199=)	rs771056622	0.00004
NM_000891.3(KCNJ2):c.1035C>T (p.His345=)	rs201747514	0.00001
NM_000891.3(KCNJ2):c.138C>T (p.Arg46=)	rs997406384	0.00001
NM_000891.3(KCNJ2):c.303T>C (p.Cys101=)	rs376921497	0.00001
NM_000891.3(KCNJ2):c.*10del	rs750011371
NM_000891.3(KCNJ2):c.1717_1721del	rs35753731
NM_000891.3(KCNJ2):c.*1721del	rs35753731
NM_000891.3(KCNJ2):c.-216-7C>A	rs2144375995
NM_000891.3(KCNJ2):c.267C>T (p.Cys89=)	rs2074386028
NM_000891.3(KCNJ2):c.774C>T (p.Ile258=)	rs1057524125

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