List of variants in gene RECQL4 reported as benign for female reproductive organ cancer

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_004260.4(RECQL4):c.1345A>C (p.Thr449Pro)	rs535692036	0.00013
NM_004260.4(RECQL4):c.646G>A (p.Glu216Lys)	rs201301365	0.00009
NM_004260.4(RECQL4):c.215C>T (p.Ala72Val)	rs763453097	0.00005
NM_004260.4(RECQL4):c.3347C>T (p.Pro1116Leu)	rs368671582	0.00005
NM_004260.4(RECQL4):c.1060G>A (p.Val354Ile)	rs551940973	0.00004
NM_004260.4(RECQL4):c.1321C>T (p.Pro441Ser)	rs557142414	0.00004
NM_004260.4(RECQL4):c.3218C>T (p.Thr1073Ile)	rs775225569	0.00004
NM_004260.4(RECQL4):c.1780G>A (p.Ala594Thr)	rs376364416	0.00002
NM_004260.4(RECQL4):c.280C>T (p.Pro94Ser)	rs1359100897	0.00002
NM_004260.4(RECQL4):c.2830C>T (p.His944Tyr)	rs527454830	0.00001
NM_004260.4(RECQL4):c.626G>A (p.Arg209Lys)	rs753018522	0.00001
NM_004260.4(RECQL4):c.682C>T (p.Leu228Phe)	rs1316434470	0.00001
NM_004260.4(RECQL4):c.988G>A (p.Ala330Thr)	rs757933716	0.00001
NM_004260.4(RECQL4):c.3284A>G (p.Glu1095Gly)

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