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Variant (rsID / SNP)

rs1053807

FAM166C

rs1053807 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM166C. Location: chromosome 2, position 26,800,422. The table records no clinical significance for this variant.

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Reference-table entries

FAM166CNot classified
Variant type
missense_variant
Chromosome / position
2:26800422
HGVS
NM_001322426.2,c.349G>A,p.Gly117Arg
Allele change
Synonymous_T129T

Public references

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