Variant (rsID / SNP)

rs191277311

rs191277311 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EIF2AK3. Location: chromosome 2, position 88,890,410. Clinical significance in the table: Uncertain significance.

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Reference-table entries

EIF2AK3Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 2:88890410
Cytoband: 2p11.2
HGVS: NM_004836.7(EIF2AK3):c.928A>T (p.Ile310Leu)
Allele change: Missense_I159L

Associated conditions / phenotypes

Monogenic diabetes|Wolcott-Rallison dysplasia

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.