List of variants in gene HSF4 reported as benign for cataract

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001374675.1(HSF4):c.123+9C>T	rs115335849	0.04892
NM_001374675.1(HSF4):c.*89G>T	rs11642409	0.00612
NM_001374675.1(HSF4):c.1414A>G (p.Ile472Val)	rs201011907	0.00303
NM_001374675.1(HSF4):c.636G>T (p.Met212Ile)	rs199742128	0.00196
NM_001374675.1(HSF4):c.561+4T>G	rs180744555	0.00158
NM_001374675.1(HSF4):c.63C>A (p.Leu21=)	rs372135101	0.00041
NM_001374675.1(HSF4):c.627-11C>T	rs199856104	0.00034
NM_001374675.1(HSF4):c.*8C>T	rs372224972	0.00026
NM_001374675.1(HSF4):c.680C>A (p.Thr227Asn)	rs200708134	0.00025
NM_001374675.1(HSF4):c.1476C>A (p.Pro492=)	rs367756178	0.00016
NM_001374675.1(HSF4):c.347G>A (p.Arg116His)	rs79121622	0.00009
NM_001374675.1(HSF4):c.991G>A (p.Ala331Thr)	rs199773890	0.00009
NM_001374675.1(HSF4):c.259G>A (p.Glu87Lys)	rs367654370	0.00007
NM_001374675.1(HSF4):c.1315C>T (p.Pro439Ser)	rs777720209	0.00001
NM_001374675.1(HSF4):c.1395C>A (p.Gly465=)	rs28364624	0.00001
NM_001374675.1(HSF4):c.1341C>G (p.Leu447=)	rs35750776
NM_001374675.1(HSF4):c.1475C>A (p.Pro492His)	rs182365484

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