List of variants in gene KCNJ10 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_002241.5(KCNJ10):c.53G>A (p.Arg18Gln)	rs115466046	0.01096
NM_002241.5(KCNJ10):c.735C>G (p.Asp245Glu)	rs146426296	0.00155
NM_002241.5(KCNJ10):c.136G>A (p.Asp46Asn)	rs141553756	0.00146
NM_002241.5(KCNJ10):c.530A>G (p.Glu177Gly)	rs145947380	0.00043
NM_002241.5(KCNJ10):c.219G>A (p.Ala73=)	rs144495959	0.00016
NM_002241.5(KCNJ10):c.240C>T (p.Phe80=)	rs774758209	0.00005
NM_002241.5(KCNJ10):c.-43G>A	rs372841245	0.00004
NM_002241.5(KCNJ10):c.927C>T (p.Tyr309=)	rs775091787	0.00002
NM_002241.5(KCNJ10):c.501G>A (p.Ala167=)	rs200522826	0.00001

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