Variant (rsID / SNP)

rs1801262

rs1801262 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NEUROD1. Location: chromosome 2, position 182,543,455. Clinical significance in the table: Benign.

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Reference-table entries

NEUROD1Benign

Clinical significance (as recorded): Benign
Variant type: missense_variant
Chromosome / position: 2:182543455
HGVS: NM_002500.5,c.133A>G,p.Thr45Ala
Allele change: Silent

Associated conditions / phenotypes

Maturity-Onset Diabetes of the Young, Type 6|Maturity-Onset Diabetes of the Young|Type 2 Diabetes Mellitus|Monogenic Diabetes|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.