Variant (rsID / SNP)

rs220126

rs220126 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UMODL1. Location: chromosome 21, position 43,531,008. The table records no clinical significance for this variant.

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Reference-table entries

UMODL1Not classified

Variant type: missense_variant
Chromosome / position: 21:43531008
HGVS: NM_173568.4,c.1676T>C,p.Met559Thr
Allele change: Missense_M487T

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.