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Variant (rsID / SNP)

rs9614382

EFCAB6

rs9614382 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EFCAB6. Location: chromosome 22, position 43,976,396. The table records no clinical significance for this variant.

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Reference-table entries

EFCAB6Not classified
Variant type
missense_variant
Chromosome / position
22:43976396
HGVS
NM_022785.4,c.3176C>T,p.Ala1059Val
Allele change
Missense_A907V

Public references

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