Variant (rsID / SNP)

rs1189466

rs1189466 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCC4. Location: chromosome 13, position 95,726,541. The table records no clinical significance for this variant.

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Reference-table entries

ABCC4Not classified

Variant type: synonymous_variant
Chromosome / position: 13:95726541
HGVS: NM_005845.5,c.2844T>C,p.Phe948Phe
Allele change: Synonymous_F948F

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.