Variant (rsID / SNP)

rs4875060

rs4875060 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCRIB. Location: chromosome 8, position 144,894,496. The table records no clinical significance for this variant.

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Reference-table entries

SCRIBNot classified

Variant type: synonymous_variant
Chromosome / position: 8:144894496
HGVS: NM_182706.5,c.846C>T,p.Thr282Thr
Allele change: Synonymous_T282T

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.