Variant (rsID / SNP)

rs34871377

rs34871377 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC37A4. Location: chromosome 11, position 118,895,632. Clinical significance in the table: Benign.

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Reference-table entries

SLC37A4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:118895632
Cytoband: 11q23.3
HGVS: NM_001164277.2(SLC37A4):c.1278G>A (p.Lys426=)
Allele change: Synonymous_K426K

Associated conditions / phenotypes

Glucose-6-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.