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Variant (rsID / SNP)

rs6604561

SPATA17

rs6604561 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPATA17. Location: chromosome 1, position 217,947,738. The table records no clinical significance for this variant.

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Reference-table entries

SPATA17Not classified
Variant type
synonymous_variant
Chromosome / position
1:217947738
HGVS
NM_001375655.1,c.582G>A,p.Gln194Gln
Allele change
Synonymous_Q194Q

Public references

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