Variant (rsID / SNP)

rs6558702

rs6558702 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CSMD1. Location: chromosome 8, position 2,909,992. The table records no clinical significance for this variant.

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Reference-table entries

CSMD1Not classified

Variant type: missense_variant
Chromosome / position: 8:2909992
HGVS: NM_033225.6,c.7652C>T,p.Thr2551Met
Allele change: Missense_T2551M

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.