List of variants in gene TRPM4 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_017636.4(TRPM4):c.301G>A (p.Ala101Thr)	rs113984787	0.00662
NM_017636.4(TRPM4):c.306T>G (p.Val102=)	rs111783027	0.00662
NM_017636.4(TRPM4):c.755G>A (p.Arg252His)	rs146564314	0.00453
NM_017636.4(TRPM4):c.870C>T (p.Asn290=)	rs141997826	0.00389
NM_017636.4(TRPM4):c.1682A>C (p.Asp561Ala)	rs56355369	0.00373
NM_017636.4(TRPM4):c.2209G>A (p.Gly737Arg)	rs145847114	0.00165
NM_017636.4(TRPM4):c.988G>A (p.Glu330Lys)	rs145771389	0.00118
NM_017636.4(TRPM4):c.2254C>T (p.Gln752Ter)	rs769917929	0.00041
NM_017636.4(TRPM4):c.308A>G (p.Tyr103Cys)	rs144781529	0.00041
NM_017636.4(TRPM4):c.1242T>C (p.Phe414=)	rs200633475	0.00031
NM_017636.4(TRPM4):c.748C>T (p.Arg250Cys)	rs144208673	0.00021
NM_017636.4(TRPM4):c.1082T>G (p.Leu361Arg)	rs148763371	0.00019

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