Variant (rsID / SNP)

rs9898

rs9898 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HRG. Location: chromosome 3, position 186,390,627. The table records no clinical significance for this variant.

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Reference-table entries

HRGNot classified

Variant type: missense_variant
Chromosome / position: 3:186390627
HGVS: NM_000412.5,c.610C>T,p.Pro204Ser
Allele change: Missense_P204S

Associated conditions / phenotypes

Rapidly Involuting Congenital Hemangioma|Thrombosis

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.