List of variants in gene APOL1 reported as uncertain significance for Focal segmental glomerulosclerosis 4, susceptibility to

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_003661.4(APOL1):c.797T>G (p.Leu266Arg)	rs142955744	0.00032
NM_003661.4(APOL1):c.1150A>T (p.Ile384Phe)	rs373463596	0.00019
NM_003661.4(APOL1):c.856C>G (p.Leu286Val)	rs755351451	0.00011
NM_003661.4(APOL1):c.967G>C (p.Glu323Gln)	rs200395416	0.00008
NM_003661.4(APOL1):c.1051T>C (p.Tyr351His)	rs375837468	0.00005
NM_003661.4(APOL1):c.334C>T (p.Arg112Cys)	rs146078613	0.00001
NM_003661.4(APOL1):c.1048G>A (p.Val350Ile)	rs2146313032
NM_003661.4(APOL1):c.1181C>G (p.Ala394Gly)	rs138178894
NM_003661.4(APOL1):c.649A>C (p.Thr217Pro)
NM_003661.4(APOL1):c.733A>G (p.Ile245Val)

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