Variant (rsID / SNP)

rs2011951

rs2011951 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC25A39. Location: chromosome 17, position 42,398,052. The table records no clinical significance for this variant.

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Reference-table entries

SLC25A39Not classified

Variant type: missense_variant
Chromosome / position: 17:42398052
HGVS: NM_001143780.3,c.739T>C,p.Phe247Leu
Allele change: Missense_F245L

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.