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Variant (rsID / SNP)

rs2241571

PRDM10

rs2241571 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRDM10. Location: chromosome 11, position 129,794,950. The table records no clinical significance for this variant.

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Reference-table entries

PRDM10Not classified
Variant type
missense_variant
Chromosome / position
11:129794950
HGVS
NM_020228.3,c.1717A>G,p.Thr573Ala
Allele change
Missense_T573A

Public references

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