Variant (rsID / SNP)

rs140343844

rs140343844 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UBN2. Location: chromosome 7, position 138,946,363. The table records no clinical significance for this variant.

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Reference-table entries

UBN2Not classified

Variant type: missense_variant
Chromosome / position: 7:138946363
HGVS: NM_173569.4,c.1271C>T,p.Ser424Leu
Allele change: Missense_S424L

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.