Variant (rsID / SNP)

rs7916519

rs7916519 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTF1A. Location: chromosome 10, position 23,466,734. Clinical significance in the table: Benign.

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Reference-table entries

PTF1ABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:23466734
Cytoband: 10p12.2
HGVS: NC_000010.10:g.23466734G>A

Associated conditions / phenotypes

Type 2 diabetes mellitus

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.