Variant (rsID / SNP)

rs2351528

rs2351528 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD109. Location: chromosome 6, position 74,497,009. The table records no clinical significance for this variant.

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Reference-table entries

CD109Not classified

Variant type: missense_variant
Chromosome / position: 6:74497009
HGVS: NM_133493.5,c.2390A>G,p.Asn797Ser
Allele change: Missense_N797S

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.