Variant (rsID / SNP)

rs34795598

rs34795598 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GAREM1. Location: chromosome 18, position 29,848,028. The table records no clinical significance for this variant.

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Reference-table entries

GAREM1Not classified

Variant type: missense_variant
Chromosome / position: 18:29848028
HGVS: NM_001242409.2,c.2437A>G,p.Ile813Val
Allele change: Missense_I812V

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.