ClinVar Miner

List of variants in gene ABCD1 reported as benign by GeneDx

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 20
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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.1780+322A>C rs11156606 0.27371
NM_000033.4(ABCD1):c.900+137C>G rs12006790 0.26526
NM_000033.4(ABCD1):c.1635-125C>T rs4148036 0.09238
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.1488+134C>T rs142236904 0.06404
NM_000033.4(ABCD1):c.1781-106G>T rs189770856 0.04701
NM_000033.4(ABCD1):c.1781-59G>A rs181218840 0.02587
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.707G>A (p.Arg236His) rs201455322 0.00114
NM_000033.4(ABCD1):c.945G>A (p.Ser315=) rs145545199 0.00037
NM_000033.4(ABCD1):c.1489-24C>G rs149185761
NM_000033.4(ABCD1):c.1489-6del rs398123101

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