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Variant (rsID / SNP)

rs8065903

SPATA20

rs8065903 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPATA20. Location: chromosome 17, position 48,629,458. The table records no clinical significance for this variant.

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Reference-table entries

SPATA20Not classified
Variant type
missense_variant
Chromosome / position
17:48629458
HGVS
NM_022827.4,c.1874A>G,p.Lys625Arg
Allele change
Missense_K609R

Public references

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