Variant (rsID / SNP)

rs35010541

rs35010541 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC37A4. Location: chromosome 11, position 118,895,635. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

SLC37A4Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 11:118895635
Cytoband: 11q23.3
HGVS: NM_001164277.2(SLC37A4):c.1275C>T (p.Ser425=)
Allele change: Synonymous_S425S

Associated conditions / phenotypes

Glucose-6-phosphate transport defect|Phosphate transport defect

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.