Variant (rsID / SNP)

rs10088378

rs10088378 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CSMD1. Location: chromosome 8, position 3,265,590. The table records no clinical significance for this variant.

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Reference-table entries

CSMD1Not classified

Variant type: synonymous_variant
Chromosome / position: 8:3265590
HGVS: NM_033225.6,c.1902G>A,p.Gln634Gln
Allele change: Synonymous_Q634Q

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.