List of variants in gene KCNJ10 reported as uncertain significance for thyroid gland disorder

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_002241.5(KCNJ10):c.1043G>A (p.Arg348His)	rs146396982	0.00034
NM_002241.5(KCNJ10):c.148C>T (p.Leu50Phe)	rs773510302	0.00019
NM_002241.5(KCNJ10):c.1102G>C (p.Glu368Gln)	rs377330985	0.00013
NM_002241.5(KCNJ10):c.*52G>A	rs148441646	0.00007
NM_002241.5(KCNJ10):c.83G>A (p.Arg28Gln)	rs766560083	0.00004
NM_002241.5(KCNJ10):c.2675_2676del	rs886045398	0.00002
NM_002241.5(KCNJ10):c.241C>T (p.Leu81Phe)	rs939420346	0.00002
NM_002241.5(KCNJ10):c.541T>C (p.Phe181Leu)	rs374746230	0.00002
NM_002241.5(KCNJ10):c.689G>A (p.Arg230Gln)	rs200807361	0.00002
NM_002241.5(KCNJ10):c.*2530G>C	rs886045400	0.00001
NM_002241.5(KCNJ10):c.*783A>G	rs886045409	0.00001
NM_002241.5(KCNJ10):c.1051G>A (p.Asp351Asn)	rs373899425	0.00001
NM_002241.5(KCNJ10):c.1140A>T (p.Ter380Cys)	rs1648596230	0.00001
NM_002241.5(KCNJ10):c.133G>A (p.Ala45Thr)	rs750246232	0.00001
NM_002241.5(KCNJ10):c.385A>G (p.Ile129Val)	rs751625111	0.00001
NM_002241.5(KCNJ10):c.427G>A (p.Ala143Thr)	rs796052607	0.00001
NM_002241.5(KCNJ10):c.511C>T (p.Arg171Trp)	rs769666695	0.00001
NM_002241.5(KCNJ10):c.635A>G (p.Gln212Arg)	rs36040296	0.00001
NM_002241.5(KCNJ10):c.652C>T (p.Leu218Phe)	rs558502886	0.00001
NM_002241.5(KCNJ10):c.79C>T (p.Arg27Trp)	rs769464065	0.00001
NM_002241.5(KCNJ10):c.*1970GT[21]	rs56656397
NM_002241.5(KCNJ10):c.*1970GT[22]	rs56656397
NM_002241.5(KCNJ10):c.*1970GT[24]	rs56656397
NM_002241.5(KCNJ10):c.*1970GT[27]	rs56656397
NM_002241.5(KCNJ10):c.*1970GT[28]	rs56656397
NM_002241.5(KCNJ10):c.*2459T>G	rs532869749
NM_002241.5(KCNJ10):c.178A>G (p.Ile60Val)	rs1648629565
NM_002241.5(KCNJ10):c.248G>C (p.Gly83Ala)	rs17853258
NM_002241.5(KCNJ10):c.5C>G (p.Thr2Arg)	rs1378425325
NM_002241.5(KCNJ10):c.934_935delinsTT (p.Thr312Leu)	rs1571265205

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