Variant (rsID / SNP)

rs3803568

rs3803568 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LMAN1L. Location: chromosome 15, position 75,108,636. The table records no clinical significance for this variant.

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Reference-table entries

LMAN1LNot classified

Variant type: missense_variant
Chromosome / position: 15:75108636
HGVS: NM_021819.3,c.314G>A,p.Arg105Gln
Allele change: Missense_R105Q

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.