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Variant (rsID / SNP)

rs3205525

FYTTD1

rs3205525 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FYTTD1. Location: chromosome 3, position 197,495,334. The table records no clinical significance for this variant.

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Reference-table entries

FYTTD1Not classified
Variant type
missense_variant
Chromosome / position
3:197495334
HGVS
NM_032288.7,c.260G>A,p.Arg87His
Allele change
Missense_R61H

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.