Variant (rsID / SNP)

rs2241400

rs2241400 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HSH2D, RAB8A. Location: chromosome 19, position 16,240,727. The table records no clinical significance for this variant.

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Reference-table entries

HSH2DNot classified

Variant type: upstream_gene_variant
Chromosome / position: 19:16240727
HGVS: NR_111904.2,n.-4111T>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.