Variant (rsID / SNP)

rs2272011

rs2272011 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCARF1. Location: chromosome 17, position 1,542,190. The table records no clinical significance for this variant.

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Reference-table entries

SCARF1Not classified

Variant type: missense_variant
Chromosome / position: 17:1542190
HGVS: NM_003693.4,c.1274C>T,p.Ala425Val
Allele change: Silent

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.