Variant (rsID / SNP)

rs34191159

rs34191159 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LTN1. Location: chromosome 21, position 30,339,120. The table records no clinical significance for this variant.

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Reference-table entries

LTN1Not classified

Variant type: missense_variant
Chromosome / position: 21:30339120
HGVS: NM_015565.3,c.1693G>T,p.Gly565Cys
Allele change: Missense_G611C

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.