RS1048661 LOXL1

Health Risk Chr 15:73927204 snv missense variant
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What This Variant Does
"rs1048661, also known as R141L, a SNP causing an amino acid change in the lysyl oxidase 1 LOXL1 gene...
Associated Conditions
GWAS Studies (9)
Trait Risk Allele OR / Beta P-value Study
Hand grip strength (baseline) G β: 0.012 2E-15 PubMed
Descending aorta maximum area (MTAG) G OR: 4.23 7E-14 PubMed
Descending aorta maximum area G OR: 4.22 1E-13 PubMed
Descending thoracic aortic diameter G β: 0.038 2E-11 PubMed
Descending thoracic aortic diameter G β: 0.039 1E-10 PubMed
Descending aorta diameter G β: 0.035 6E-10 PubMed
Carpal tunnel syndrome T OR: 0.96 8E-10 PubMed
Descending aorta minimum area OR: 3.86 4E-9 PubMed
Descending aorta minimum area OR: 4.7 2E-8 PubMed
Population Frequencies
gnomAD ALL
0%
1kG AFR
84.6%
1kG ALL
31.1%
1kG AMR
30.5%
1kG EAS
51.8%
1kG EUR
68%
1kG SAS
30.7%
Other Variants in LOXL1
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