Variant (rsID / SNP)

rs7813902

rs7813902 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MBOAT4, LEPROTL1. Location: chromosome 8, position 29,996,256. The table records no clinical significance for this variant.

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Reference-table entries

MBOAT4Not classified

Variant type: missense_variant
Chromosome / position: 8:29996256
HGVS: NM_001100916.2,c.136A>G,p.Thr46Ala
Allele change: Missense_T46A

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.