List of variants in gene TRPM2 reported as 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_003307.4(TRPM2):c.3796-6C>T	rs117548537	0.00365
NM_003307.4(TRPM2):c.3777C>T (p.Asn1259=)	rs140290337	0.00253
NM_003307.4(TRPM2):c.4040C>T (p.Thr1347Met)	rs45589233	0.00160
NM_003307.4(TRPM2):c.1923C>G (p.Ile641Met)	rs150484698	0.00150
NM_003307.4(TRPM2):c.1805T>C (p.Val602Ala)	rs149930126	0.00138
NM_003307.4(TRPM2):c.3784G>A (p.Val1262Met)	rs150071509	0.00111
NM_003307.4(TRPM2):c.3653C>A (p.Ala1218Glu)
NM_003307.4(TRPM2):c.3684_3710del (p.Arg1228_Asp1236del)
NM_003307.4(TRPM2):c.3797C>T (p.Thr1266Met)	rs144380426

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