Variant (rsID / SNP)

rs60782127

rs60782127 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCC1. Location: chromosome 16, position 16,142,079. Clinical significance in the table: Benign.

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Reference-table entries

ABCC1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 16:16142079
Cytoband: 16p13.11
HGVS: NM_004996.4(ABCC1):c.1299G>T (p.Arg433Ser)
Allele change: Missense_R433S

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.