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Variant (rsID / SNP)

rs7185

FARSB

rs7185 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FARSB. Location: chromosome 2, position 223,436,607. The table records no clinical significance for this variant.

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Reference-table entries

FARSBNot classified
Variant type
missense_variant
Chromosome / position
2:223436607
HGVS
NM_005687.5,c.1753G>A,p.Val585Ile
Allele change
Silent

Public references

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