Variant (rsID / SNP)

rs11698812

rs11698812 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RBPJL. Location: chromosome 20, position 43,948,221. Clinical significance in the table: Benign.

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Reference-table entries

RBPJLBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 20:43948221
Cytoband: 20q13.12
HGVS: NC_000020.10:g.43948221A>C

Associated conditions / phenotypes

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.