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Variant (rsID / SNP)

rs61733632

FAM120B

rs61733632 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM120B. Location: chromosome 6, position 170,627,174. The table records no clinical significance for this variant.

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Reference-table entries

FAM120BNot classified
Variant type
synonymous_variant
Chromosome / position
6:170627174
HGVS
NM_001286380.2,c.765C>T,p.Asp255Asp
Allele change
Synonymous_D244D

Public references

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