Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs6425977

THRAP3

rs6425977 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to THRAP3. Location: chromosome 1, position 36,752,433. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

THRAP3Not classified
Variant type
missense_variant
Chromosome / position
1:36752433
HGVS
NM_001321471.2,c.602C>T,p.Ala201Val
Allele change
Missense_A201V

Public references

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