Variant (rsID / SNP)

rs512253

rs512253 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OBSCN. Location: chromosome 1, position 228,560,700. The table records no clinical significance for this variant.

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Reference-table entries

OBSCNNot classified

Variant type: synonymous_variant
Chromosome / position: 1:228560700
HGVS: NM_001386125.1,c.25092T>C,p.Asp8364Asp
Allele change: Synonymous_D8364D

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.