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Variant (rsID / SNP)

rs35027739

CRTAC1

rs35027739 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CRTAC1. Location: chromosome 10, position 99,696,003. The table records no clinical significance for this variant.

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Reference-table entries

CRTAC1Not classified
Variant type
synonymous_variant
Chromosome / position
10:99696003
HGVS
NM_018058.7,c.345C>T,p.Ile115Ile
Allele change
Synonymous_I115I

Public references

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