Variant (rsID / SNP)

rs12769244

rs12769244 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MARCHF8. Location: chromosome 10, position 45,959,385. The table records no clinical significance for this variant.

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Reference-table entries

MARCHF8Not classified

Variant type: missense_variant
Chromosome / position: 10:45959385
HGVS: NM_001282866.2,c.302C>T,p.Ser101Leu
Allele change: Silent

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.