Variant (rsID / SNP)

rs7978353

rs7978353 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MLXIP. Location: chromosome 12, position 122,617,989. The table records no clinical significance for this variant.

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Reference-table entries

MLXIPNot classified

Variant type: missense_variant
Chromosome / position: 12:122617989
HGVS: NM_014938.6,c.1187A>G,p.Glu396Gly
Allele change: Missense_E396G

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.