ClinVar Miner

List of variants studied for hypochromic microcytic anemia by Genome-Nilou Lab

Included ClinVar conditions (3):

Iron deficiency anemia
Microcytic anemia with liver iron overload
Severe congenital hypochromic anemia with ringed sideroblasts

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000617.3(SLC11A2):c.1576-14A>G	rs161044	0.90828
NM_000617.3(SLC11A2):c.35-498A>C	rs445520	0.90819
NM_000617.3(SLC11A2):c.309+44A>C	rs224589

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