Variant (rsID / SNP)

rs35332062

rs35332062 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MLXIPL. Location: chromosome 7, position 73,012,042. The table records no clinical significance for this variant.

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Reference-table entries

MLXIPLNot classified

Variant type: missense_variant&splice_region_variant
Chromosome / position: 7:73012042
HGVS: NM_032951.3,c.1073C>T,p.Ala358Val
Allele change: Missense_A358V

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.