Variant (rsID / SNP)

rs13116684

rs13116684 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NIPAL1. Location: chromosome 4, position 48,037,926. The table records no clinical significance for this variant.

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Reference-table entries

NIPAL1Not classified

Variant type: missense_variant
Chromosome / position: 4:48037926
HGVS: NM_207330.3,c.970A>G,p.Ile324Val
Allele change: Missense_I324V

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.