Variant (rsID / SNP)

rs3087689

rs3087689 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRI1. Location: chromosome 19, position 10,664,632. The table records no clinical significance for this variant.

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Reference-table entries

KRI1Not classified

Variant type: missense_variant
Chromosome / position: 19:10664632
HGVS: NM_023008.5,c.2107T>C,p.Ser703Pro
Allele change: Missense_S709P

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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