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Variant (rsID / SNP)

rs4666689

FSIP2

rs4666689 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FSIP2. Location: chromosome 2, position 186,670,979. The table records no clinical significance for this variant.

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Reference-table entries

FSIP2Not classified
Variant type
missense_variant
Chromosome / position
2:186670979
HGVS
NM_173651.4,c.16946T>C,p.Ile5649Thr
Allele change
Missense_I5649T

Public references

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