List of variants in gene HCFC1 reported as benign by Eurofins NTD LLC (GA)

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_005334.3(HCFC1):c.5859C>T (p.Cys1953=)	rs3027875	0.42119
NM_005334.3(HCFC1):c.2841A>G (p.Pro947=)	rs730106	0.37791
NM_005334.3(HCFC1):c.3490T>C (p.Ser1164Pro)	rs1051152	0.37778
NM_005334.3(HCFC1):c.713-13C>T	rs59607260	0.19358
NM_005334.3(HCFC1):c.4185G>A (p.Ala1395=)	rs2071133	0.19260
NM_005334.3(HCFC1):c.2283C>G (p.Thr761=)	rs2071134	0.15977
NM_005334.3(HCFC1):c.1085-12G>A	rs3027893	0.04847
NM_005334.3(HCFC1):c.4545G>A (p.Pro1515=)	rs1051153	0.03363
NM_005334.3(HCFC1):c.3568G>A (p.Gly1190Ser)	rs185987427	0.01804
NM_005334.3(HCFC1):c.2872A>G (p.Thr958Ala)	rs3027884	0.00091

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