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Variant (rsID / SNP)

rs7599598

FER1L5

rs7599598 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FER1L5. Location: chromosome 2, position 97,351,840. The table records no clinical significance for this variant.

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Reference-table entries

FER1L5Not classified
Variant type
missense_variant
Chromosome / position
2:97351840
HGVS
NM_001293083.2,c.2059A>G,p.Thr687Ala
Allele change
Missense_T687A

Public references

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