Variant (rsID / SNP)

rs6555335

rs6555335 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADAMTS16. Location: chromosome 5, position 5,200,281. The table records no clinical significance for this variant.

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Reference-table entries

ADAMTS16Not classified

Variant type: synonymous_variant
Chromosome / position: 5:5200281
HGVS: NM_139056.4,c.1350C>T,p.Cys450Cys
Allele change: Synonymous_C450C

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.