Variant (rsID / SNP)

rs61853459

rs61853459 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PANK1. Location: chromosome 10, position 91,405,044. The table records no clinical significance for this variant.

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Reference-table entries

PANK1Not classified

Variant type: upstream_gene_variant
Chromosome / position: 10:91405044
HGVS: NM_148977.3,c.-396G>A
Allele change: Missense_G6S

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.