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Variant (rsID / SNP)

rs9475077

FAM83B

rs9475077 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM83B. Location: chromosome 6, position 54,806,489. The table records no clinical significance for this variant.

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Reference-table entries

FAM83BNot classified
Variant type
missense_variant
Chromosome / position
6:54806489
HGVS
NM_001010872.3,c.2720C>A,p.Thr907Asn
Allele change
Missense_T907N

Public references

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