List of variants in gene HAMP reported as pathogenic for disorder of metabolite absorption and transport

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_021175.4(HAMP):c.-25G>A	rs944843686	0.00001
NM_021175.4(HAMP):c.166C>T (p.Arg56Ter)	rs104894695
NM_021175.4(HAMP):c.176G>C (p.Arg59Pro)	rs2066319871
NM_021175.4(HAMP):c.95del (p.Gly32fs)	rs1189025914

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