List of variants in gene TRPM6 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_017662.4(TRPM6):c.-167A>C	rs77048628	0.02299
NM_017662.4(TRPM6):c.-163A>G	rs73538241	0.02297
NM_017662.5(TRPM6):c.2428C>T (p.Leu810=)	rs55956641	0.01104
NM_017662.5(TRPM6):c.4569A>T (p.Thr1523=)	rs150409948	0.00610
NM_017662.5(TRPM6):c.*1222C>T	rs190131362	0.00291
NM_017662.5(TRPM6):c.511G>A (p.Gly171Arg)	rs150874152	0.00278
NM_017662.5(TRPM6):c.633T>C (p.Gly211=)	rs144221623	0.00259
NM_017662.5(TRPM6):c.1014G>T (p.Met338Ile)	rs56155062	0.00211
NM_017662.5(TRPM6):c.*1160C>T	rs563649179	0.00118
NM_017662.5(TRPM6):c.*670A>C	rs144874847	0.00072
NM_017662.5(TRPM6):c.*1784A>G	rs143290917	0.00055
NM_017662.5(TRPM6):c.*96C>G	rs369609402	0.00034
NM_017662.5(TRPM6):c.2649T>C (p.Ala883=)	rs373991938	0.00016
NM_017662.5(TRPM6):c.622C>A (p.Pro208Thr)	rs755626959	0.00006
NM_017662.5(TRPM6):c.*235C>T	rs527880339
NM_017662.5(TRPM6):c.*710AT[3]	rs201267884
NM_017662.5(TRPM6):c.*919G>T	rs371692085

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