Variant (rsID / SNP)

rs17079099

rs17079099 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CSMD1. Location: chromosome 8, position 2,879,070. The table records no clinical significance for this variant.

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Reference-table entries

CSMD1Not classified

Variant type: intron_variant
Chromosome / position: 8:2879070
HGVS: NM_033225.6,c.7856-2898G>A
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.