Variant (rsID / SNP)

rs9813017

rs9813017 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDCD6IP. Location: chromosome 3, position 33,893,987. The table records no clinical significance for this variant.

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Reference-table entries

PDCD6IPNot classified

Variant type: missense_variant
Chromosome / position: 3:33893987
HGVS: NM_001162429.3,c.1664A>G,p.Asn555Ser
Allele change: Missense_N555S

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.