List of variants in gene TMPRSS6 reported as benign by PreventionGenetics, part of Exact Sciences

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001374504.1(TMPRSS6):c.2180T>C (p.Val727Ala)	rs855791	0.64686
NM_001374504.1(TMPRSS6):c.1536C>T (p.Asp512=)	rs4820268	0.59140
NM_001374504.1(TMPRSS6):c.2190C>T (p.Tyr730=)	rs2235321	0.40210
NM_001374504.1(TMPRSS6):c.730A>G (p.Lys244Glu)	rs2235324	0.39823
NM_001374504.1(TMPRSS6):c.1056G>A (p.Ser352=)	rs2111833	0.34630
NM_001374504.1(TMPRSS6):c.72G>A (p.Pro24=)	rs11704654	0.17025
NM_001374504.1(TMPRSS6):c.1227C>T (p.Tyr409=)	rs881144	0.08889
NM_001374504.1(TMPRSS6):c.-1-107C>T	rs115270691	0.02489
NM_001374504.1(TMPRSS6):c.1441+10C>T	rs79816125	0.01239
NM_001374504.1(TMPRSS6):c.2356G>A (p.Val786Ile)	rs139105452	0.00876
NM_001374504.1(TMPRSS6):c.2105G>T (p.Arg702Leu)	rs115310908	0.00447
NM_001374504.1(TMPRSS6):c.2112C>T (p.Gly704=)	rs118004991	0.00361
NM_001374504.1(TMPRSS6):c.1842-31CCCCA[5]	rs60484081
NM_001374504.1(TMPRSS6):c.1842-31CCCCA[8]	rs60484081
NM_001374504.1(TMPRSS6):c.2113+458G>C

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