List of variants reported as benign for Bietti crystalline corneoretinal dystrophy by Illumina Laboratory Services, Illumina

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Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_207352.4(CYP4V2):c.*1781A>C	rs6842047	0.89083
NM_207352.4(CYP4V2):c.*725C>T	rs10033577	0.89040
NM_207352.3(CYP4V2):c.-296A>C	rs7662717	0.86820
NM_207352.4(CYP4V2):c.*741C>T	rs10033581	0.81342
NM_207352.4(CYP4V2):c.810T>G (p.Ala270=)	rs3736455	0.62273
NM_207352.4(CYP4V2):c.775C>A (p.Gln259Lys)	rs13146272	0.60911
NM_207352.4(CYP4V2):c.64C>G (p.Leu22Val)	rs1055138	0.46276
NM_207352.4(CYP4V2):c.*1236A>T	rs1053094	0.45426
NM_207352.4(CYP4V2):c.-146C>T	rs1398007	0.41622
NM_207352.4(CYP4V2):c.-152A>G	rs2241819	0.39682
NM_207352.4(CYP4V2):c.802-7C>T	rs3817184	0.36293
NM_207352.4(CYP4V2):c.*2399C>T	rs56413992	0.15680
NM_207352.4(CYP4V2):c.846T>C (p.Cys282=)	rs3736456	0.07854
NM_207352.4(CYP4V2):c.1083C>T (p.Asp361=)	rs10029149	0.07706
NM_207352.4(CYP4V2):c.*1148A>G	rs10011736	0.07494
NM_207352.4(CYP4V2):c.327+11G>C	rs62350517	0.05079
NM_207352.4(CYP4V2):c.555A>T (p.Ala185=)	rs11932764	0.04735
NM_207352.4(CYP4V2):c.823G>A (p.Glu275Lys)	rs34745240	0.03921
NM_207352.4(CYP4V2):c.1536C>T (p.Gly512=)	rs72646298	0.01209
NM_207352.4(CYP4V2):c.-128A>G	rs531909464	0.01113
NM_207352.4(CYP4V2):c.*2106G>T	rs72646302	0.01061
NM_207352.4(CYP4V2):c.24C>T (p.Leu8=)	rs202148693	0.00077
NM_207352.4(CYP4V2):c.*2303G>C	rs576134216	0.00006
NM_207352.4(CYP4V2):c.*2166C>G	rs192436436	0.00001
NM_207352.4(CYP4V2):c.*1027C>T	rs541778964
NM_207352.4(CYP4V2):c.*364T>G	rs7697077

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