Variant (rsID / SNP)

rs1885986

rs1885986 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SMG6. Location: chromosome 17, position 2,203,175. The table records no clinical significance for this variant.

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Reference-table entries

SMG6Not classified

Variant type: missense_variant
Chromosome / position: 17:2203175
HGVS: NM_017575.5,c.872G>C,p.Arg291Pro
Allele change: Missense_R291P

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.