Variant (rsID / SNP)

rs12750774

rs12750774 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TDRD10. Location: chromosome 1, position 154,516,477. The table records no clinical significance for this variant.

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Reference-table entries

TDRD10Not classified

Variant type: missense_variant
Chromosome / position: 1:154516477
HGVS: NM_001098475.2,c.542G>A,p.Arg181Gln
Allele change: Missense_R181Q

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.