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Variant (rsID / SNP)

rs17826498

FSIP2

rs17826498 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FSIP2. Location: chromosome 2, position 186,671,256. The table records no clinical significance for this variant.

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Reference-table entries

FSIP2Not classified
Variant type
synonymous_variant
Chromosome / position
2:186671256
HGVS
NM_173651.4,c.17223T>C,p.Asn5741Asn
Allele change
Synonymous_N5741N

Public references

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