Variant (rsID / SNP)

rs2280851

rs2280851 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HHLA1. Location: chromosome 8, position 133,089,975. The table records no clinical significance for this variant.

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Reference-table entries

HHLA1Not classified

Variant type: missense_variant&splice_region_variant
Chromosome / position: 8:133089975
HGVS: NM_001145095.3,c.1169T>C,p.Leu390Ser
Allele change: Missense_L390S

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.