Variant (rsID / SNP)

rs11101675

rs11101675 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADAM8. Location: chromosome 10, position 135,087,460. The table records no clinical significance for this variant.

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Reference-table entries

ADAM8Not classified

Variant type: missense_variant
Chromosome / position: 10:135087460
HGVS: NM_001109.5,c.301G>A,p.Gly101Arg
Allele change: Missense_G101R

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.