Variant (rsID / SNP)

rs1553316

rs1553316 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HAVCR1. Location: chromosome 5, position 156,479,509. The table records no clinical significance for this variant.

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Reference-table entries

HAVCR1Not classified

Variant type: missense_variant
Chromosome / position: 5:156479509
HGVS: NM_001308156.2,c.536T>C,p.Leu179Pro
Allele change: Missense_L179P

Associated conditions / phenotypes

Multiple Sclerosis

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.