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Variant (rsID / SNP)

rs75991134

CPAMD8

rs75991134 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CPAMD8. Location: chromosome 19, position 17,104,379. The table records no clinical significance for this variant.

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Reference-table entries

CPAMD8Not classified
Variant type
synonymous_variant
Chromosome / position
19:17104379
HGVS
NM_015692.5,c.1113C>T,p.Pro371Pro
Allele change
Synonymous_P418P

Public references

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