Variant (rsID / SNP)

rs4842838

rs4842838 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADAMTSL3. Location: chromosome 15, position 84,582,124. The table records no clinical significance for this variant.

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Reference-table entries

ADAMTSL3Not classified

Variant type: missense_variant
Chromosome / position: 15:84582124
HGVS: NM_207517.3,c.1981G>T,p.Val661Leu
Allele change: Missense_V661L

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.