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Variant (rsID / SNP)

rs2277033

PRDM10

rs2277033 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRDM10. Location: chromosome 11, position 129,801,043. The table records no clinical significance for this variant.

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Reference-table entries

PRDM10Not classified
Variant type
synonymous_variant
Chromosome / position
11:129801043
HGVS
NM_020228.3,c.1398G>A,p.Gln466Gln
Allele change
Synonymous_Q466Q

Public references

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