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Variant (rsID / SNP)

rs239798

FAM83B

rs239798 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM83B. Location: chromosome 6, position 54,805,688. The table records no clinical significance for this variant.

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Reference-table entries

FAM83BNot classified
Variant type
missense_variant
Chromosome / position
6:54805688
HGVS
NM_001010872.3,c.1919A>C,p.Lys640Thr
Allele change
Missense_K640T

Public references

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