Variant (rsID / SNP)

rs116698870

rs116698870 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HPS1. Location: chromosome 10, position 100,177,957. Clinical significance in the table: Uncertain significance.

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Reference-table entries

HPS1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 10:100177957
Cytoband: 10q24.2
HGVS: NM_000195.5(HPS1):c.1915G>A (p.Gly639Ser)
Allele change: Missense_G315S

Associated conditions / phenotypes

Hermansky-Pudlak syndrome

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.