List of variants in gene KCNJ2 reported as benign by Invitae

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.1065T>G (p.Leu355=)	rs139564374	0.00073
NM_000891.3(KCNJ2):c.213C>T (p.Asp71=)	rs150671256	0.00070
NM_000891.3(KCNJ2):c.1044C>T (p.Tyr348=)	rs146330042	0.00049
NM_000891.3(KCNJ2):c.372C>T (p.Ser124=)	rs138877244	0.00024
NM_000891.3(KCNJ2):c.96C>T (p.Asn32=)	rs67120636	0.00005
NM_000891.3(KCNJ2):c.225G>A (p.Thr75=)	rs192172778	0.00003
NM_000891.3(KCNJ2):c.531C>T (p.Gly177=)	rs544384907	0.00002
NM_000891.3(KCNJ2):c.1035C>T (p.His345=)	rs201747514	0.00001

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