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Variant (rsID / SNP)

rs61730035

SLC37A4

rs61730035 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC37A4. Location: chromosome 11, position 118,895,962. 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
11:118895962
Cytoband
11q23.3
HGVS
NM_001164277.2(SLC37A4):c.1062C>T (p.Asn354=)
Allele change
Synonymous_N354N

Associated conditions / phenotypes

Glucose-6-phosphate transport defect|Glycogen storage disease due to glucose-6-phosphatase deficiency type IA|Phosphate transport defect

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.