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Variant (rsID / SNP)

rs3010877

AADACL3

rs3010877 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AADACL3. Location: chromosome 1, position 12,779,618. The table records no clinical significance for this variant.

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Reference-table entries

AADACL3Not classified
Variant type
missense_variant
Chromosome / position
1:12779618
HGVS
NM_001103170.3,c.310T>C,p.Ser104Pro
Allele change
Missense_S104P

Public references

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