Variant (rsID / SNP)

rs7141840

rs7141840 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MIA2. Location: chromosome 14, position 39,703,324. The table records no clinical significance for this variant.

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Reference-table entries

MIA2Not classified

Variant type: synonymous_variant
Chromosome / position: 14:39703324
HGVS: NM_001329214.4,c.6A>G,p.Ala2Ala
Allele change: Synonymous_A2A

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.