Variant (rsID / SNP)

rs9376173

rs9376173 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDE7B. Location: chromosome 6, position 136,359,446. The table records no clinical significance for this variant.

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Reference-table entries

PDE7BNot classified

Variant type: intron_variant
Chromosome / position: 6:136359446
HGVS: NM_018945.4,c.83-70423A>C
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.