Variant: rs1557055405 

    present in Gene: ABCD1
    present in Chromosome: X
    Position on Chromosome: 153743532
    Alleles of this Variant: T/A

rs1557055405 in ABCD1 gene and Adrenoleukodystrophy PMID 22071894 2012 Clinical utility gene card for: adrenoleukodystrophy.

PMID 9452087 1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.

rs1557055405 in ABCD1 gene and Ankle clonus PMID 9452087 1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.

rs1557055405 in ABCD1 gene and Asthma PMID 9452087 1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.

rs1557055405 in ABCD1 gene and Babinski Reflex PMID 9452087 1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.

rs1557055405 in ABCD1 gene and Brisk reflexes PMID 9452087 1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.

rs1557055405 in ABCD1 gene and Gait abnormality PMID 9452087 1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.

rs1557055405 in ABCD1 gene and High, narrow palate PMID 9452087 1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.

rs1557055405 in ABCD1 gene and Impaired distal proprioception PMID 9452087 1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.

rs1557055405 in ABCD1 gene and Impaired pain sensation PMID 9452087 1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.

rs1557055405 in ABCD1 gene and Impaired vibration sensation in the lower limbs PMID 9452087 1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.

rs1557055405 in ABCD1 gene and Low Back Pain PMID 9452087 1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.

rs1557055405 in ABCD1 gene and Lower limb hyperreflexia PMID 9452087 1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.

rs1557055405 in ABCD1 gene and Progressive spastic paraplegia PMID 9452087 1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.

rs1557055405 in ABCD1 gene and Progressive spasticity PMID 9452087 1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.

rs1557055405 in ABCD1 gene and Romberg's sign positive PMID 9452087 1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.

rs1557055405 in ABCD1 gene and Scoliosis, unspecified PMID 9452087 1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.

rs1557055405 in ABCD1 gene and Serum lipids high (finding) PMID 9452087 1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.

rs1557055405 in ABCD1 gene and Thoracolumbar scoliosis PMID 9452087 1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.

rs1557055405 in ABCD1 gene and Urgency of micturition PMID 9452087 1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.

rs1557055405 in ABCD1 gene and Urinary Stress Incontinence PMID 9452087 1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.

rs1557055405 in ABCD1 gene and Very long chain fatty acid accumulation PMID 9452087 1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.