Variant (rsID / SNP)

rs17074425

rs17074425 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EFCAB9. Location: chromosome 5, position 171,627,701. The table records no clinical significance for this variant.

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Reference-table entries

EFCAB9Not classified

Variant type: synonymous_variant
Chromosome / position: 5:171627701
HGVS: NM_001171183.2,c.417G>A,p.Gln139Gln
Allele change: Synonymous_Q139Q

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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