Variant (rsID / SNP)

rs35478105

rs35478105 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADAMTS18. Location: chromosome 16, position 77,325,325. The table records no clinical significance for this variant.

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Reference-table entries

ADAMTS18Not classified

Variant type: missense_variant
Chromosome / position: 16:77325325
HGVS: NM_199355.4,c.3240C>A,p.Ser1080Arg
Allele change: Missense_S1080R

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.