Variant (rsID / SNP)

rs11541836

rs11541836 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DOLPP1. Location: chromosome 9, position 131,846,957. The table records no clinical significance for this variant.

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Reference-table entries

DOLPP1Not classified

Variant type: synonymous_variant
Chromosome / position: 9:131846957
HGVS: NM_020438.5,c.87T>C,p.Ser29Ser
Allele change: Silent

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.