Variant (rsID / SNP)

rs3811448

rs3811448 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TDRD10. Location: chromosome 1, position 154,516,578. The table records no clinical significance for this variant.

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Reference-table entries

TDRD10Not classified

Variant type: missense_variant
Chromosome / position: 1:154516578
HGVS: NM_001098475.2,c.643G>A,p.Val215Ile
Allele change: Missense_V215I

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.