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Variant (rsID / SNP)

rs3770657

ETAA1

rs3770657 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ETAA1. Location: chromosome 2, position 67,630,980. The table records no clinical significance for this variant.

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Reference-table entries

ETAA1Not classified
Variant type
missense_variant
Chromosome / position
2:67630980
HGVS
NM_019002.4,c.1166G>A,p.Ser389Asn
Allele change
Missense_S389N

Public references

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