Variant (rsID / SNP)

rs13235543

rs13235543 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MLXIPL. Location: chromosome 7, position 73,013,901. The table records no clinical significance for this variant.

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Reference-table entries

MLXIPLNot classified

Variant type: synonymous_variant
Chromosome / position: 7:73013901
HGVS: NM_032951.3,c.1026G>A,p.Pro342Pro
Allele change: Synonymous_P342P

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.