Variant (rsID / SNP)

rs2304103

rs2304103 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAAP24. Location: chromosome 19, position 33,467,413. The table records no clinical significance for this variant.

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Reference-table entries

FAAP24Not classified

Variant type: missense_variant
Chromosome / position: 19:33467413
HGVS: NM_152266.5,c.473C>T,p.Ser158Leu
Allele change: Missense_S63L

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.