List of variants in gene ABCD1 reported as benign 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: 18

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HGVS	dbSNP	gnomAD frequency
NM_000033.4(ABCD1):c.*8G>C	rs2229539	0.70012
NM_000033.3(ABCD1):c.*1035C>T	rs6643782	0.69879
NM_000033.4(ABCD1):c.*877C>T	rs11803	0.46252
NM_000033.4(ABCD1):c.*894G>A	rs1055847	0.44006
NM_000033.4(ABCD1):c.*608G>A	rs73640819	0.19859
NM_000033.4(ABCD1):c.-59C>T	rs4148030	0.09150
NM_000033.4(ABCD1):c.1548G>A (p.Leu516=)	rs41314153	0.08321
NM_000033.4(ABCD1):c.2019C>T (p.Phe673=)	rs76637913	0.01192
NM_000033.4(ABCD1):c.901-10C>T	rs2269365	0.00512
NM_000033.4(ABCD1):c.-202C>G	rs781978041	0.00067
NM_000033.4(ABCD1):c.*985C>G	rs782309410	0.00063
NM_000033.4(ABCD1):c.258C>T (p.Val86=)	rs200660869	0.00061
NM_000033.4(ABCD1):c.1047C>A (p.Val349=)	rs185931852	0.00034
NM_000033.4(ABCD1):c.1810G>A (p.Val604Ile)	rs151201945	0.00033
NM_000033.4(ABCD1):c.1354C>T (p.Arg452Trp)	rs368061976	0.00012
NM_000033.4(ABCD1):c.*473C>T	rs782343473	0.00011
NM_000033.4(ABCD1):c.768C>T (p.Asn256=)	rs782236148	0.00003
NM_000033.4(ABCD1):c.2043C>T (p.Phe681=)	rs782327280

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