Variant (rsID / SNP)

rs1863968

rs1863968 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADAMTS16. Location: chromosome 5, position 5,146,395. The table records no clinical significance for this variant.

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Reference-table entries

ADAMTS16Not classified

Variant type: missense_variant
Chromosome / position: 5:5146395
HGVS: NM_139056.4,c.328A>G,p.Met110Val
Allele change: Missense_M110V

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.