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Variant (rsID / SNP)

rs4753069

FAT3

rs4753069 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAT3. Location: chromosome 11, position 92,590,448. The table records no clinical significance for this variant.

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Reference-table entries

FAT3Not classified
Variant type
missense_variant
Chromosome / position
11:92590448
HGVS
NM_001367949.2,c.11434A>G,p.Ser3812Gly
Allele change
Missense_S3812G

Public references

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