List of variants in gene SLC11A1 studied for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000578.4(SLC11A1):c.1328T>C (p.Val443Ala)	rs17215556	0.00708
NM_000578.4(SLC11A1):c.501-4T>G	rs17221980	0.00498
NM_000578.4(SLC11A1):c.1048G>A (p.Val350Met)	rs141861983	0.00233
NM_000578.4(SLC11A1):c.522C>T (p.Val174=)	rs139234551	0.00192
NM_000578.4(SLC11A1):c.1165-7A>C	rs17221987	0.00141
NM_000578.4(SLC11A1):c.1492G>A (p.Gly498Ser)	rs142636978	0.00141
NM_000578.4(SLC11A1):c.36G>A (p.Gly12=)	rs17221910	0.00020
NM_000578.4(SLC11A1):c.1255C>A (p.Arg419=)	rs147071155	0.00019
NM_000578.4(SLC11A1):c.984C>A (p.His328Gln)	rs377625960	0.00005
NM_000578.4(SLC11A1):c.1045-7C>T	rs373819173	0.00002
NM_000578.4(SLC11A1):c.571+8C>T	rs1178711277	0.00002
NM_000578.4(SLC11A1):c.811C>T (p.Arg271Trp)	rs765411619	0.00002
NM_000578.4(SLC11A1):c.1450G>C (p.Val484Leu)	rs138316650
NM_000578.4(SLC11A1):c.324A>T (p.Arg108=)	rs775281462
NM_000578.4(SLC11A1):c.943A>C (p.Asn315His)	rs2106334814

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