Variant (rsID / SNP)

rs3745245

rs3745245 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRI1. Location: chromosome 19, position 10,676,423. The table records no clinical significance for this variant.

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Reference-table entries

KRI1Not classified

Variant type: synonymous_variant
Chromosome / position: 19:10676423
HGVS: NM_023008.5,c.138C>T,p.Ser46Ser
Allele change: Synonymous_S52S

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.