Variant (rsID / SNP)

rs3757241

rs3757241 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC25A27. Location: chromosome 6, position 46,623,698. The table records no clinical significance for this variant.

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Reference-table entries

SLC25A27Not classified

Variant type: synonymous_variant
Chromosome / position: 6:46623698
HGVS: NM_004277.5,c.225T>C,p.Ala75Ala
Allele change: Synonymous_A75A

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.