List of variants in gene TRPM4 reported as likely benign by Illumina Laboratory Services, Illumina

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_017636.4(TRPM4):c.2934T>C (p.Ile978=)	rs35516880	0.02629
NM_017636.4(TRPM4):c.1050+13_1050+16dup	rs137898843	0.02485
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.3082C>T (p.Leu1028=)	rs79286201	0.01125
NM_017636.4(TRPM4):c.322C>T (p.Arg108Cys)	rs115335683	0.01074
NM_017636.4(TRPM4):c.448+6C>T	rs78051297	0.01005
NM_017636.4(TRPM4):c.2953+15G>A	rs115274216	0.00850
NM_017636.4(TRPM4):c.2619C>T (p.Thr873=)	rs144544237	0.00790
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.618G>A (p.Ser206=)	rs142788545	0.00422
NM_017636.4(TRPM4):c.1682A>C (p.Asp561Ala)	rs56355369	0.00373
NM_017636.4(TRPM4):c.449-14C>T	rs112328642	0.00356
NM_017636.4(TRPM4):c.3427A>G (p.Ser1143Gly)	rs138603244	0.00198
NM_017636.4(TRPM4):c.1575G>A (p.Trp525Ter)	rs71352737	0.00168
NM_017636.4(TRPM4):c.878A>G (p.Gln293Arg)	rs172147855	0.00004
NM_017636.4(TRPM4):c.243G>A (p.Thr81=)	rs375928899

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