Variant (rsID / SNP)

rs55758736

rs55758736 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BLK. Location: chromosome 8, position 11,405,576. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

BLKBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 8:11405576
Cytoband: 8p23.1
HGVS: NM_001715.3(BLK):c.211G>A (p.Ala71Thr)
Allele change: Silent

Associated conditions / phenotypes

Maturity-onset diabetes of the young type 11|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.