Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs35665085

HDHD5

rs35665085 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HDHD5. Location: chromosome 22, position 17,625,915. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

HDHD5Not classified
Variant type
missense_variant&splice_region_variant
Chromosome / position
22:17625915
HGVS
NM_033070.3,c.536C>T,p.Thr179Met
Allele change
Missense_T179M

Public references

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