List of variants in gene FANCI reported as likely benign by Sema4, Sema4

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: 23

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HGVS	dbSNP	gnomAD frequency
NM_001113378.2(FANCI):c.2997C>T (p.Ser999=)	rs138675752	0.00248
NM_001113378.2(FANCI):c.3592-8T>C	rs185599057	0.00200
NM_001113378.2(FANCI):c.2487T>G (p.Leu829=)	rs145762491	0.00155
NM_001113378.2(FANCI):c.3865A>G (p.Ile1289Val)	rs114549781	0.00150
NM_001113378.2(FANCI):c.2817G>T (p.Lys939Asn)	rs145192583	0.00147
NM_001113378.2(FANCI):c.3660T>C (p.Ser1220=)	rs116380142	0.00131
NM_001113378.2(FANCI):c.753C>T (p.Asp251=)	rs151169233	0.00124
NM_001113378.2(FANCI):c.1491A>G (p.Gln497=)	rs145349375	0.00083
NM_001113378.2(FANCI):c.158G>C (p.Gly53Ala)	rs149223439	0.00028
NM_001113378.2(FANCI):c.528A>G (p.Gln176=)	rs145939211	0.00027
NM_001113378.2(FANCI):c.1749T>C (p.Phe583=)	rs201037656	0.00024
NM_001113378.2(FANCI):c.1963G>A (p.Gly655Arg)	rs138026584	0.00019
NM_001113378.2(FANCI):c.446-6T>G	rs377255054	0.00015
NM_001113378.2(FANCI):c.2406T>C (p.Asp802=)	rs147934193	0.00013
NM_001113378.2(FANCI):c.2646A>G (p.Leu882=)	rs199627578	0.00012
NM_001113378.2(FANCI):c.2097C>T (p.Tyr699=)	rs148415946	0.00004
NM_001113378.2(FANCI):c.2685G>A (p.Ser895=)	rs145665176	0.00004
NM_001113378.2(FANCI):c.3705C>T (p.Ala1235=)	rs185771112	0.00004
NM_001113378.2(FANCI):c.1134T>C (p.Val378=)	rs1201574474
NM_001113378.2(FANCI):c.1263C>A (p.Leu421=)	rs376956791
NM_001113378.2(FANCI):c.1617G>A (p.Gly539=)	rs757928977
NM_001113378.2(FANCI):c.2430G>A (p.Val810=)	rs2151741501
NM_001113378.2(FANCI):c.3291A>G (p.Glu1097=)	rs2054690236

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