Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs112812449

RIPK1

rs112812449 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RIPK1. Location: chromosome 6, position 3,090,990. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

RIPK1Not classified
Variant type
intron_variant
Chromosome / position
6:3090990
HGVS
NM_001354930.2,c.915+1099C>T
Allele change
Silent

Public references

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