List of variants in gene ABCD1 reported as benign by Genome-Nilou Lab

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_000033.4(ABCD1):c.*8G>C	rs2229539	0.70012
NM_000033.4(ABCD1):c.1992-32C>T	rs4898368	0.59030
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.1393+31C>T	rs73633774	0.01908
NM_000033.4(ABCD1):c.2019C>T (p.Phe673=)	rs76637913	0.01192
NM_000033.4(ABCD1):c.901-16C>T	rs41302176	0.00840
NM_000033.4(ABCD1):c.901-10C>T	rs2269365	0.00512
NM_000033.4(ABCD1):c.471A>G (p.Gln157=)	rs151148684	0.00506
NM_000033.4(ABCD1):c.696G>T (p.Ala232=)	rs147595334	0.00357
NM_000033.4(ABCD1):c.38A>C (p.Asn13Thr)	rs183021839	0.00235
NM_000033.4(ABCD1):c.707G>A (p.Arg236His)	rs201455322	0.00114
NM_000033.4(ABCD1):c.258C>T (p.Val86=)	rs200660869	0.00061
NM_000033.4(ABCD1):c.757C>G (p.Leu253Val)	rs150151955	0.00060
NM_000033.4(ABCD1):c.601G>A (p.Val201Met)	rs139415350	0.00048
NM_000033.4(ABCD1):c.945G>A (p.Ser315=)	rs145545199	0.00037
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.181G>A (p.Ala61Thr)	rs782134465	0.00028
NM_000033.4(ABCD1):c.1455A>C (p.Ser485=)	rs150878397	0.00019
NM_000033.4(ABCD1):c.1215G>A (p.Ser405=)	rs138233092	0.00018
NM_000033.4(ABCD1):c.901-5C>T	rs782603062	0.00015
NM_000033.4(ABCD1):c.1354C>T (p.Arg452Trp)	rs368061976	0.00012
NM_000033.4(ABCD1):c.768C>T (p.Asn256=)	rs782236148	0.00003
NM_000033.4(ABCD1):c.1744G>A (p.Val582Ile)	rs76180859	0.00001
NM_000033.4(ABCD1):c.1092C>G (p.Ala364=)	rs782250326
NM_000033.4(ABCD1):c.1489-24C>G	rs149185761
NM_000033.4(ABCD1):c.1489-6del	rs398123101
NM_000033.4(ABCD1):c.1748T>A (p.Val583Glu)	rs79383557
NM_000033.4(ABCD1):c.1823G>A (p.Gly608Asp)	rs78993751
NM_000033.4(ABCD1):c.2043C>T (p.Phe681=)	rs782327280

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