Variant (rsID / SNP)

rs13394

rs13394 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PIH1D1. Location: chromosome 19, position 49,950,298. The table records no clinical significance for this variant.

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Reference-table entries

PIH1D1Not classified

Variant type: missense_variant
Chromosome / position: 19:49950298
HGVS: NM_017916.3,c.670G>A,p.Val224Ile
Allele change: Missense_V224I

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.