Variant (rsID / SNP)

rs3739014

rs3739014 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TBC1D8. Location: chromosome 2, position 101,638,888. The table records no clinical significance for this variant.

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Reference-table entries

TBC1D8Not classified

Variant type: synonymous_variant
Chromosome / position: 2:101638888
HGVS: NM_001330348.2,c.2616T>C,p.Asp872Asp
Allele change: Silent

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.