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Variant (rsID / SNP)

rs2275720

ADAM8

rs2275720 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADAM8. Location: chromosome 10, position 135,082,346. The table records no clinical significance for this variant.

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Reference-table entries

ADAM8Not classified
Variant type
missense_variant
Chromosome / position
10:135082346
HGVS
NM_001109.5,c.1969T>C,p.Phe657Leu
Allele change
Missense_F657L

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.