Variant (rsID / SNP)

rs1169310

rs1169310 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HNF1A. Location: chromosome 12, position 121,439,433. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

HNF1ABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:121439433
Cytoband: 12q24.31
HGVS: NM_000545.8(HNF1A):c.*438G>A
Allele change: Silent

Associated conditions / phenotypes

Maturity-onset diabetes of the young type 3|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.