List of variants in gene CD58 reported as uncertain significance for not specified

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001779.3(CD58):c.101A>G (p.Tyr34Cys)	rs762708999	0.00005
NM_001779.3(CD58):c.745T>G (p.Ser249Ala)	rs376792396	0.00004
NM_001779.3(CD58):c.626G>A (p.Ser209Asn)	rs758492590	0.00003
NM_001779.3(CD58):c.320C>T (p.Ser107Leu)	rs1266661778	0.00001
NM_001779.3(CD58):c.257T>A (p.Val86Glu)
NM_001779.3(CD58):c.313A>G (p.Met105Val)
NM_001779.3(CD58):c.328A>G (p.Ile110Val)	rs376614019
NM_001779.3(CD58):c.404A>C (p.Asn135Thr)
NM_001779.3(CD58):c.487A>G (p.Met163Val)	rs2525018997
NM_001779.3(CD58):c.670G>T (p.Ala224Ser)
NM_001779.3(CD58):c.71G>T (p.Gly24Val)
NM_001779.3(CD58):c.736A>G (p.Arg246Gly)	rs2526148843
NM_001779.3(CD58):c.93A>C (p.Gln31His)

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