Variant (rsID / SNP)

rs10927387

rs10927387 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EFCAB2. Location: chromosome 1, position 245,245,402. The table records no clinical significance for this variant.

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Reference-table entries

EFCAB2Not classified

Variant type: synonymous_variant
Chromosome / position: 1:245245402
HGVS: NM_001290327.2,c.231C>T,p.Pro77Pro
Allele change: Synonymous_P67P

Associated conditions / phenotypes

Neutropenia|Lung Cancer

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.