List of variants in gene TRPM6 reported as benign for intestinal hypomagnesemia 1

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_017662.5(TRPM6):c.2124T>G (p.Leu708=)	rs7859201	0.46572
NM_017662.5(TRPM6):c.954C>T (p.Gly318=)	rs7018994	0.28712
NM_017662.5(TRPM6):c.1443+42A>G	rs4300062	0.27612
NM_017662.5(TRPM6):c.4750A>G (p.Lys1584Glu)	rs2274924	0.22975
NM_017662.5(TRPM6):c.2442G>A (p.Gln814=)	rs4145894	0.15921
NM_017662.5(TRPM6):c.4764T>C (p.Asn1588=)	rs2274925	0.14509
NM_017662.5(TRPM6):c.4177G>A (p.Val1393Ile)	rs3750425	0.14052
NM_017662.5(TRPM6):c.1872T>C (p.Ala624=)	rs12349050	0.09732
NM_017662.5(TRPM6):c.5776+23A>G	rs506973	0.09571
NM_017662.5(TRPM6):c.1851G>A (p.Leu617=)	rs11144089	0.07757
NM_017662.5(TRPM6):c.1639C>T (p.His547Tyr)	rs115354606	0.02960
NM_017662.5(TRPM6):c.4221C>T (p.His1407=)	rs56331140	0.02029
NM_017662.5(TRPM6):c.3514C>A (p.Arg1172=)	rs35904059	0.01376
NM_017662.5(TRPM6):c.1207+6T>C	rs139475376	0.01166
NM_017662.5(TRPM6):c.3821A>G (p.Gln1274Arg)	rs34608911	0.00853
NM_017662.5(TRPM6):c.*913T>C	rs113586292	0.00659
NM_017662.5(TRPM6):c.4988A>G (p.Gln1663Arg)	rs55679040	0.00650
NM_017662.5(TRPM6):c.*1084C>T	rs184870782	0.00391
NM_017662.5(TRPM6):c.4707A>T (p.Ala1569=)	rs34550263	0.00375
NM_017662.5(TRPM6):c.1450G>A (p.Gly484Arg)	rs77826848	0.00360
NM_017662.5(TRPM6):c.268A>T (p.Ser90Cys)	rs145791687	0.00280
NM_017662.5(TRPM6):c.3486G>A (p.Met1162Ile)	rs139669465	0.00028
NM_017662.5(TRPM6):c.*238G>A	rs11144075
NM_017662.5(TRPM6):c.*788AT[8]	rs143924458
NM_017662.5(TRPM6):c.6033G>A (p.Thr2011=)	rs139342869

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