Variant (rsID / SNP)

rs9891498

rs9891498 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MARCHF10. Location: chromosome 17, position 60,814,273. The table records no clinical significance for this variant.

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Reference-table entries

MARCHF10Not classified

Variant type: missense_variant
Chromosome / position: 17:60814273
HGVS: NM_001288779.2,c.1070T>C,p.Phe357Ser
Allele change: Missense_F319S

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.