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Variant (rsID / SNP)

rs9646748

MFSD6

rs9646748 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MFSD6. Location: chromosome 2, position 191,301,368. The table records no clinical significance for this variant.

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Reference-table entries

MFSD6Not classified
Variant type
missense_variant
Chromosome / position
2:191301368
HGVS
NM_001375986.1,c.613A>G,p.Arg205Gly
Allele change
Missense_R205G

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.