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Variant (rsID / SNP)

rs4661330

FHAD1

rs4661330 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FHAD1. Location: chromosome 1, position 15,687,059. The table records no clinical significance for this variant.

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Reference-table entries

FHAD1Not classified
Variant type
missense_variant
Chromosome / position
1:15687059
HGVS
NM_001391957.1,c.2822A>G,p.Glu941Gly
Allele change
Missense_E919G

Public references

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