List of variants in gene SLC27A4 reported as benign for not provided

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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: 21

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HGVS	dbSNP	gnomAD frequency
NM_005094.4(SLC27A4):c.625G>A (p.Gly209Ser)	rs2240953	0.08653
NM_005094.4(SLC27A4):c.1774+147G>A	rs2003560	0.05710
NM_005094.4(SLC27A4):c.1052A>G (p.Asn351Ser)	rs111417655	0.02275
NM_005094.4(SLC27A4):c.362G>A (p.Arg121Gln)	rs56224008	0.01813
NM_005094.4(SLC27A4):c.988-5C>T	rs183007998	0.00479
NM_005094.4(SLC27A4):c.1035A>G (p.Pro345=)	rs55976774	0.00462
NM_005094.4(SLC27A4):c.785+7G>A	rs17848328	0.00291
NM_005094.4(SLC27A4):c.716-15G>A	rs17848327	0.00202
NM_005094.4(SLC27A4):c.1545C>T (p.Asn515=)	rs2240952	0.00120
NM_005094.4(SLC27A4):c.167G>T (p.Gly56Val)	rs140481562	0.00066
NM_005094.4(SLC27A4):c.492T>C (p.Ala164=)	rs139914381	0.00035
NM_005094.4(SLC27A4):c.314G>A (p.Arg105His)	rs142664086	0.00029
NM_005094.4(SLC27A4):c.411T>C (p.Asn137=)	rs142183053	0.00015
NM_005094.4(SLC27A4):c.1197+17G>A
NM_005094.4(SLC27A4):c.1325-79del	rs139411337
NM_005094.4(SLC27A4):c.161+17G>T
NM_005094.4(SLC27A4):c.1627+19G>A
NM_005094.4(SLC27A4):c.168C>T (p.Gly56=)
NM_005094.4(SLC27A4):c.1775-12C>T
NM_005094.4(SLC27A4):c.556+16del
NM_005094.4(SLC27A4):c.716-18C>A	rs201333290

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