List of variants in gene TRPM4 reported as likely benign for keratosis

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_017636.4(TRPM4):c.2535C>G (p.Pro845=)	rs560849729	0.00015
NM_017636.4(TRPM4):c.345G>A (p.Pro115=)	rs750991001	0.00003
NM_017636.4(TRPM4):c.582C>A (p.Val194=)	rs914389404	0.00003
NM_017636.4(TRPM4):c.1893T>C (p.Tyr631=)	rs765927799	0.00001
NM_017636.4(TRPM4):c.2205T>C (p.Pro735=)	rs200681329	0.00001
NM_017636.4(TRPM4):c.2895C>T (p.Arg965=)	rs1271791433	0.00001
NM_017636.4(TRPM4):c.3329-8C>G	rs369748756

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