Variant (rsID / SNP)

rs117518215

rs117518215 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADAMTS12. Location: chromosome 5, position 33,881,252. The table records no clinical significance for this variant.

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Reference-table entries

ADAMTS12Not classified

Variant type: missense_variant
Chromosome / position: 5:33881252
HGVS: NM_030955.4,c.461C>T,p.Thr154Met
Allele change: Missense_T154M

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.