Variant (rsID / SNP)

rs760202

rs760202 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HADH. Location: chromosome 4, position 108,911,018. Clinical significance in the table: Benign.

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Reference-table entries

HADHBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:108911018
Cytoband: 4q25
HGVS: NM_005327.4(HADH):c.-71C>T
Allele change: Silent

Associated conditions / phenotypes

Hyperinsulinemic hypoglycemia, familial, 4|Deficiency of 3-hydroxyacyl-CoA dehydrogenase

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.