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Variant (rsID / SNP)

rs116087774

RIPK1

rs116087774 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RIPK1. Location: chromosome 6, position 3,090,895. The table records no clinical significance for this variant.

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Reference-table entries

RIPK1Not classified
Variant type
intron_variant
Chromosome / position
6:3090895
HGVS
NM_001354930.2,c.915+1004G>A
Allele change
Silent

Public references

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