Variant (rsID / SNP)

rs4148211

rs4148211 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCG8. Location: chromosome 2, position 44,071,743. Clinical significance in the table: Benign.

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Reference-table entries

ABCG8Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:44071743
Cytoband: 2p21
HGVS: NM_022437.3(ABCG8):c.161A>G (p.Tyr54Cys)
Allele change: Missense_Y54C

Associated conditions / phenotypes

Sitosterolemia 1

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.