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Variant (rsID / SNP)

rs8418

SAMM50

rs8418 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SAMM50. Location: chromosome 22, position 44,379,838. The table records no clinical significance for this variant.

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Reference-table entries

SAMM50Not classified
Variant type
missense_variant
Chromosome / position
22:44379838
HGVS
NM_015380.5,c.1033A>G,p.Ile345Val
Allele change
Missense_I345V

Public references

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