List of variants in gene FOXRED1 reported as likely benign by GeneDx

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_017547.4(FOXRED1):c.1102-273C>A	rs113109739	0.01435
NM_017547.4(FOXRED1):c.306+71G>A	rs80037786	0.00813
NM_017547.4(FOXRED1):c.733+154G>A	rs188022599	0.00490
NC_000011.10:g.126269114C>G	rs139053088	0.00388
NM_017547.4(FOXRED1):c.86-145C>T	rs188086066	0.00334
NM_017547.4(FOXRED1):c.86-29G>T	rs200259576	0.00292
NM_017547.3(FOXRED1):c.-163G>C	rs552937899	0.00259
NM_017547.4(FOXRED1):c.-30G>A	rs201673735	0.00133
NM_017547.4(FOXRED1):c.536+9C>G	rs370312170	0.00065
NM_017547.4(FOXRED1):c.*6T>C	rs201387039	0.00026
NM_017547.4(FOXRED1):c.971+13C>T	rs374211633	0.00017
NM_017547.4(FOXRED1):c.448C>T (p.Leu150=)	rs531412126	0.00012
NM_017547.4(FOXRED1):c.909T>C (p.Gly303=)	rs768064354	0.00002
NM_017547.4(FOXRED1):c.*85T>C	rs372575072	0.00001
NM_017547.4(FOXRED1):c.307-14T>C	rs541684918	0.00001
NM_017547.4(FOXRED1):c.537-11G>A	rs199599636	0.00001
NM_017547.4(FOXRED1):c.934C>T (p.Leu312=)	rs1274929569	0.00001
NM_017547.4(FOXRED1):c.945C>T (p.Thr315=)	rs779980682	0.00001
NM_017547.4(FOXRED1):c.*93G>A	rs114082966
NM_017547.4(FOXRED1):c.1102-181del	rs202024738
NM_017547.4(FOXRED1):c.1278G>A (p.Pro426=)	rs775435796
NM_017547.4(FOXRED1):c.1404C>T (p.Pro468=)	rs1057522293
NM_017547.4(FOXRED1):c.306+322del	rs1168226778
NM_017547.4(FOXRED1):c.306+322dup	rs1168226778
NM_017547.4(FOXRED1):c.307-38G>A	rs375883538
NM_017547.4(FOXRED1):c.434T>C (p.Val145Ala)	rs863224018
NM_017547.4(FOXRED1):c.537-269del	rs60892467
NM_017547.4(FOXRED1):c.632-12T>C	rs757107408
NM_017547.4(FOXRED1):c.675G>A (p.Gln225=)	rs150562772
NM_017547.4(FOXRED1):c.852C>T (p.Cys284=)	rs546801411
NM_017547.4(FOXRED1):c.899C>G (p.Ala300Gly)	rs149851763

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