Variant (rsID / SNP)

rs60225321

rs60225321 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NPFFR1. Location: chromosome 10, position 72,014,863. The table records no clinical significance for this variant.

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Reference-table entries

NPFFR1Not classified

Variant type: synonymous_variant
Chromosome / position: 10:72014863
HGVS: NM_022146.5,c.1143C>T,p.Ser381Ser
Allele change: Synonymous_S381S

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.