List of variants in gene TRPM4 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_017636.4(TRPM4):c.1050+13_1050+16dup	rs137898843	0.02485
NM_017636.4(TRPM4):c.267+14C>G	rs113040724	0.02235
NM_017636.4(TRPM4):c.449-10G>A	rs78444754	0.02013
NM_017636.4(TRPM4):c.783G>A (p.Lys261=)	rs111930830	0.01836
NM_017636.4(TRPM4):c.3641-19C>G	rs7256050	0.01753
NM_017636.4(TRPM4):c.3082C>T (p.Leu1028=)	rs79286201	0.01125
NM_017636.4(TRPM4):c.322C>T (p.Arg108Cys)	rs115335683	0.01074
NM_017636.4(TRPM4):c.755G>A (p.Arg252His)	rs146564314	0.00453
NM_017636.4(TRPM4):c.3405A>C (p.Ala1135=)	rs144647383	0.00450
NM_017636.4(TRPM4):c.870C>T (p.Asn290=)	rs141997826	0.00389
NM_017636.4(TRPM4):c.449-14C>T	rs112328642	0.00356
NM_017636.4(TRPM4):c.3611C>T (p.Pro1204Leu)	rs150391806	0.00310
NM_017636.4(TRPM4):c.1368C>G (p.Thr456=)	rs56118173	0.00274
NM_017636.4(TRPM4):c.2209G>A (p.Gly737Arg)	rs145847114	0.00165
NM_017636.4(TRPM4):c.1459_1494del (p.Lys487_Leu498del)	rs878855029

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