Variant (rsID / SNP)

rs4483821

rs4483821 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADAMTSL3. Location: chromosome 15, position 84,488,636. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ADAMTSL3Not classified

Variant type: missense_variant
Chromosome / position: 15:84488636
HGVS: NM_207517.3,c.437A>G,p.His146Arg
Allele change: Missense_H146R

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.