Variant (rsID / SNP)

rs73135597

rs73135597 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABI3BP. Location: chromosome 3, position 100,560,860. The table records no clinical significance for this variant.

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Reference-table entries

ABI3BPNot classified

Variant type: missense_variant
Chromosome / position: 3:100560860
HGVS: NM_001375547.2,c.1747C>T,p.Pro583Ser
Allele change: Missense_P541S

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.