Variant (rsID / SNP)

rs6795735

rs6795735 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADAMTS9-AS2. Location: chromosome 3, position 64,705,365. The table records no clinical significance for this variant.

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Reference-table entries

ADAMTS9-AS2Not classified

Variant type: single nucleotide variant
Chromosome / position: 3:64705365
Cytoband: 3p14.1
HGVS: NR_038264.1(ADAMTS9-AS2):n.469+34351C>T
Allele change: Silent

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.