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Variant (rsID / SNP)

rs9358767

GPLD1

rs9358767 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPLD1. Location: chromosome 6, position 24,445,829. The table records no clinical significance for this variant.

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Reference-table entries

GPLD1Not classified
Variant type
synonymous_variant
Chromosome / position
6:24445829
HGVS
NM_001503.4,c.1965C>T,p.His655His
Allele change
Synonymous_H655H

Public references

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