Variant (rsID / SNP)

rs1010156

rs1010156 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LOXL2. Location: chromosome 8, position 23,190,941. The table records no clinical significance for this variant.

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Reference-table entries

LOXL2Not classified

Variant type: synonymous_variant
Chromosome / position: 8:23190941
HGVS: NM_002318.3,c.939A>G,p.Ser313Ser
Allele change: Synonymous_S313S

Associated conditions / phenotypes

Aneurysm, Intracranial Berry, 12|Aneurysm

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.