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Variant (rsID / SNP)

rs16989753

SFI1

rs16989753 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SFI1. Location: chromosome 22, position 31,946,282. The table records no clinical significance for this variant.

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Reference-table entries

SFI1Not classified
Variant type
synonymous_variant
Chromosome / position
22:31946282
HGVS
NM_001007467.3,c.492T>C,p.Tyr164Tyr
Allele change
Synonymous_Y82Y

Public references

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