Variant (rsID / SNP)

rs11187583

rs11187583 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FRA10AC1. Location: chromosome 10, position 95,441,272. The table records no clinical significance for this variant.

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Reference-table entries

FRA10AC1Not classified

Variant type: missense_variant
Chromosome / position: 10:95441272
HGVS: NM_001347712.2,c.752C>T,p.Ser251Phe
Allele change: Missense_S251F

Associated conditions / phenotypes

Missense_S251F

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.