Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs35471617

COL21A1

rs35471617 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL21A1. Location: chromosome 6, position 56,033,094. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

COL21A1Not classified
Variant type
missense_variant&splice_region_variant
Chromosome / position
6:56033094
HGVS
NM_001318751.2,c.1028C>T,p.Thr343Met
Allele change
Missense_T343M

Public references

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