List of variants in gene VLDLR reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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_003383.5(VLDLR):c.982A>G (p.Ser328Gly)	rs116306908	0.00238
NM_003383.5(VLDLR):c.902G>A (p.Arg301Gln)	rs139671268	0.00141
NM_003383.5(VLDLR):c.1901G>A (p.Arg634His)	rs35339834	0.00108
NM_003383.5(VLDLR):c.1643A>G (p.Lys548Arg)	rs148487944	0.00053
NM_003383.5(VLDLR):c.2371G>A (p.Val791Ile)	rs35334949	0.00051
NM_003383.5(VLDLR):c.792C>T (p.Cys264=)	rs141850403	0.00036
NM_003383.5(VLDLR):c.1297G>A (p.Val433Met)	rs140062795	0.00026
NM_003383.5(VLDLR):c.1532A>G (p.Asn511Ser)	rs182216426	0.00026
NM_003383.5(VLDLR):c.732C>G (p.Ile244Met)	rs145995735	0.00026
NM_003383.5(VLDLR):c.1132T>C (p.Tyr378His)	rs142885301	0.00021
NM_003383.5(VLDLR):c.1838G>A (p.Arg613His)	rs35948251	0.00017
NM_003383.5(VLDLR):c.1667G>A (p.Arg556Gln)	rs746518411	0.00016
NM_003383.5(VLDLR):c.836G>A (p.Arg279Gln)	rs114307467	0.00014
NM_003383.5(VLDLR):c.315A>G (p.Pro105=)	rs138500615	0.00009
NM_003383.5(VLDLR):c.104C>T (p.Pro35Leu)	rs113809568	0.00007
NM_003383.5(VLDLR):c.1307C>A (p.Ala436Glu)	rs758404215	0.00005
NM_003383.5(VLDLR):c.746G>A (p.Gly249Asp)	rs199615969	0.00005
NM_003383.5(VLDLR):c.2546T>C (p.Ile849Thr)	rs116082439	0.00004
NM_003383.5(VLDLR):c.583G>A (p.Ala195Thr)	rs201652132	0.00004
NM_003383.5(VLDLR):c.1245C>T (p.Gly415=)	rs746308049	0.00003
NM_003383.5(VLDLR):c.494G>A (p.Arg165His)	rs532269001	0.00003
NM_003383.5(VLDLR):c.292G>A (p.Glu98Lys)	rs200596776	0.00002
NM_003383.5(VLDLR):c.1246G>A (p.Gly416Ser)	rs146889983	0.00001
NM_003383.5(VLDLR):c.1343G>A (p.Arg448Gln)	rs137946976	0.00001
NM_003383.5(VLDLR):c.1782G>A (p.Leu594=)	rs376819187	0.00001
NM_003383.5(VLDLR):c.*8G>T	rs772294761
NM_003383.5(VLDLR):c.-42GGC[9]	rs71329437
NM_003383.5(VLDLR):c.1150G>A (p.Ala384Thr)	rs1554621358
NM_003383.5(VLDLR):c.1452C>A (p.Phe484Leu)	rs144724569
NM_003383.5(VLDLR):c.2322A>T (p.Gly774=)	rs770771918
NM_003383.5(VLDLR):c.2587A>G (p.Ile863Val)	rs751464256

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