Variant (rsID / SNP)

rs11537737

rs11537737 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HNRNPU. Location: chromosome 1, position 245,018,909. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

HNRNPUBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:245018909
Cytoband: 1q44
HGVS: NM_031844.3(HNRNPU):c.2169C>T (p.Ala723=)
Allele change: Synonymous_A704A

Associated conditions / phenotypes

History of neurodevelopmental disorder|heterogeneous nuclear ribonucleoprotein G, human

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.