Variant (rsID / SNP)

rs13078867

rs13078867 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EFHB. Location: chromosome 3, position 19,962,044. The table records no clinical significance for this variant.

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Reference-table entries

EFHBNot classified

Variant type: missense_variant
Chromosome / position: 3:19962044
HGVS: NM_144715.4,c.805C>T,p.Pro269Ser
Allele change: Missense_P269S

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.