Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs10497497

TTC30A

rs10497497 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTC30A. Location: chromosome 2, position 178,481,818. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

TTC30ANot classified
Variant type
synonymous_variant
Chromosome / position
2:178481818
HGVS
NM_152275.4,c.1612C>A,p.Arg538Arg
Allele change
Synonymous_R538R

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.