List of variants in gene CYP4V2 reported as uncertain significance by Illumina Laboratory Services, Illumina

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: 36

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HGVS	dbSNP	gnomAD frequency
NM_207352.4(CYP4V2):c.*4T>C	rs76978024	0.00479
NM_207352.4(CYP4V2):c.1328G>A (p.Arg443Gln)	rs72646291	0.00306
NM_207352.4(CYP4V2):c.610G>A (p.Ala204Thr)	rs61745524	0.00292
NM_207352.4(CYP4V2):c.*160A>G	rs187506967	0.00244
NM_207352.4(CYP4V2):c.*175A>G	rs192122143	0.00193
NM_207352.4(CYP4V2):c.99G>A (p.Leu33=)	rs145611966	0.00162
NM_207352.4(CYP4V2):c.1446G>A (p.Ser482=)	rs141950964	0.00089
NM_207352.4(CYP4V2):c.282C>T (p.Val94=)	rs142775374	0.00036
NM_207352.4(CYP4V2):c.367A>G (p.Met123Val)	rs149684063	0.00027
NM_207352.4(CYP4V2):c.674+14T>C	rs201205689	0.00020
NM_207352.4(CYP4V2):c.1103G>A (p.Arg368His)	rs138739819	0.00019
NM_207352.4(CYP4V2):c.1120G>T (p.Asp374Tyr)	rs376015936	0.00013
NM_207352.4(CYP4V2):c.1289C>T (p.Pro430Leu)	rs144008429	0.00013
NM_207352.4(CYP4V2):c.1184T>C (p.Val395Ala)	rs143711287	0.00007
NM_207352.4(CYP4V2):c.1339G>A (p.Glu447Lys)	rs200623218	0.00006
NM_207352.4(CYP4V2):c.237G>T (p.Glu79Asp)	rs199476185	0.00005
NM_207352.4(CYP4V2):c.*172T>C	rs1043961395	0.00004
NM_207352.4(CYP4V2):c.163C>A (p.Arg55Ser)	rs760001831	0.00004
NM_207352.4(CYP4V2):c.662G>A (p.Arg221His)	rs763083895	0.00004
NM_207352.4(CYP4V2):c.1423A>G (p.Met475Val)	rs762821992	0.00003
NM_207352.4(CYP4V2):c.626T>C (p.Ile209Thr)	rs376640607	0.00003
NM_207352.4(CYP4V2):c.736C>G (p.Leu246Val)	rs531538384	0.00003
NM_207352.4(CYP4V2):c.1344T>C (p.Asn448=)	rs72646292	0.00002
NM_207352.4(CYP4V2):c.302C>T (p.Ala101Val)	rs143272248	0.00001
NM_207352.4(CYP4V2):c.661C>T (p.Arg221Cys)	rs745471184	0.00001
NM_207352.4(CYP4V2):c.772C>A (p.Leu258Ile)	rs761190623	0.00001
NM_207352.4(CYP4V2):c.*198A>T	rs150697121
NM_207352.4(CYP4V2):c.*204T>C	rs577711483
NM_207352.4(CYP4V2):c.1062A>G (p.Lys354=)	rs1736463662
NM_207352.4(CYP4V2):c.1091-15A>G	rs1300763823
NM_207352.4(CYP4V2):c.1225+14A>G	rs886059282
NM_207352.4(CYP4V2):c.1338C>G (p.Pro446=)	rs35524919
NM_207352.4(CYP4V2):c.1338C>T (p.Pro446=)	rs35524919
NM_207352.4(CYP4V2):c.311A>G (p.Asn104Ser)	rs886059281
NM_207352.4(CYP4V2):c.841G>A (p.Asp281Asn)	rs913510827
NM_207352.4(CYP4V2):c.987+7T>C	rs1736302352

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