List of variants reported as likely benign for Hemochromatosis type 3 by Illumina Laboratory Services, Illumina

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_003227.4(TFR2):c.2255G>A (p.Arg752His)	rs41295942	0.02204
NM_003227.4(TFR2):c.2085G>C (p.Ser695=)	rs150303632	0.01091
NM_003227.4(TFR2):c.*116C>T	rs41296648	0.00230
NM_003227.4(TFR2):c.447G>A (p.Gly149=)	rs41302366	0.00022
NM_003227.4(TFR2):c.1249A>G (p.Ile417Val)	rs141101651	0.00006

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