List of variants in gene KCNJ2 reported as benign by Ambry Genetics

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000891.3(KCNJ2):c.1146C>T (p.Leu382=)	rs173135	0.12771
NM_000891.3(KCNJ2):c.660C>T (p.Ser220=)	rs7221086	0.06793
NM_000891.3(KCNJ2):c.1045G>A (p.Glu349Lys)	rs375330016	0.00015
NM_000891.3(KCNJ2):c.1244C>T (p.Pro415Leu)	rs373799322	0.00013
NM_000891.3(KCNJ2):c.616G>A (p.Gly206Ser)	rs141035459	0.00011
NM_000891.3(KCNJ2):c.277G>A (p.Val93Ile)	rs147750704	0.00007
NM_000891.3(KCNJ2):c.973C>T (p.Arg325Cys)	rs202067116	0.00007
NM_000891.3(KCNJ2):c.359A>C (p.Lys120Thr)	rs375646186	0.00003
NM_000891.3(KCNJ2):c.128G>A (p.Cys43Tyr)	rs774424161	0.00002
NM_000891.3(KCNJ2):c.102G>C (p.Lys34Asn)	rs1476737505	0.00001

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