List of variants in gene TFR2 reported as likely benign for Hemochromatosis type 3

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: 32

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HGVS	dbSNP	gnomAD frequency
NM_003227.4(TFR2):c.714C>G (p.Ile238Met)	rs34242818	0.03989
NM_003227.4(TFR2):c.2255G>A (p.Arg752His)	rs41295942	0.02204
NM_003227.4(TFR2):c.1473G>A (p.Glu491=)	rs139178017	0.00289
NM_003227.4(TFR2):c.*116C>T	rs41296648	0.00230
NM_003227.4(TFR2):c.1762A>T (p.Met588Leu)	rs143251494	0.00123
NM_003227.4(TFR2):c.2137-5C>T	rs374964799	0.00111
NM_003227.4(TFR2):c.225G>A (p.Ala75=)	rs148140889	0.00079
NM_003227.4(TFR2):c.767T>G (p.Leu256Arg)	rs200287731	0.00062
NM_003227.4(TFR2):c.1242C>T (p.Phe414=)	rs150883560	0.00026
NM_003227.4(TFR2):c.19C>T (p.Leu7=)	rs367635364	0.00024
NM_003227.4(TFR2):c.447G>A (p.Gly149=)	rs41302366	0.00022
NM_003227.4(TFR2):c.1640A>T (p.Tyr547Phe)	rs573769443	0.00021
NM_003227.4(TFR2):c.1863C>T (p.Ala621=)	rs374489702	0.00013
NM_003227.4(TFR2):c.1305A>G (p.Ala435=)	rs372014293	0.00012
NM_003227.4(TFR2):c.1076T>A (p.Ile359Asn)	rs140020076	0.00010
NM_003227.4(TFR2):c.120C>T (p.Asp40=)	rs370005999	0.00010
NM_003227.4(TFR2):c.1179C>T (p.Pro393=)	rs149590949	0.00006
NM_003227.4(TFR2):c.1249A>G (p.Ile417Val)	rs141101651	0.00006
NM_003227.4(TFR2):c.462G>A (p.Glu154=)	rs761954336	0.00006
NM_003227.4(TFR2):c.2346G>A (p.Thr782=)	rs367723987	0.00005
NM_003227.4(TFR2):c.1193G>A (p.Arg398Gln)	rs202022975	0.00004
NM_003227.4(TFR2):c.2184G>A (p.Pro728=)	rs982999802	0.00004
NM_003227.4(TFR2):c.2268C>T (p.Ser756=)	rs760061994	0.00003
NM_003227.4(TFR2):c.1527C>T (p.Asn509=)	rs201943504	0.00001
NM_003227.4(TFR2):c.177T>C (p.Pro59=)	rs961591005	0.00001
NM_003227.4(TFR2):c.2277C>T (p.Pro759=)	rs748376968	0.00001
NM_003227.4(TFR2):c.2400C>T (p.Asn800=)	rs766681676	0.00001
NM_003227.4(TFR2):c.420C>G (p.Leu140=)	rs778911966	0.00001
NM_003227.4(TFR2):c.690C>G (p.Asp230Glu)	rs41303465	0.00001
NM_003227.4(TFR2):c.123G>C (p.Gly41=)	rs779980249
NM_003227.4(TFR2):c.1605+10C>G	rs577722163
NM_003227.4(TFR2):c.1767+7C>G	rs41295912

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