Variant (rsID / SNP)

rs61730326

rs61730326 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZFP57. Location: chromosome 6, position 29,640,802. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ZFP57Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 6:29640802
Cytoband: 6p22.1
HGVS: NM_001109809.5(ZFP57):c.1086T>C (p.Thr362=)
Allele change: Synonymous_T362T

Associated conditions / phenotypes

Diabetes mellitus, transient neonatal, 1

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.