Variant (rsID / SNP)

rs193922587

rs193922587 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HNF1A. Location: chromosome 12, position 121,437,325. Clinical significance in the table: Likely benign.

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Reference-table entries

HNF1ALikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 12:121437325
Cytoband: 12q24.31
HGVS: NM_000545.8(HNF1A):c.1663C>T (p.Leu555Phe)
Allele change: Missense_L555F

Associated conditions / phenotypes

Maturity-onset diabetes of the young type 3|Monogenic diabetes

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.