Variant (rsID / SNP)

rs474474

rs474474 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CSMD2. Location: chromosome 1, position 34,238,283. The table records no clinical significance for this variant.

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Reference-table entries

CSMD2Not classified

Variant type: missense_variant
Chromosome / position: 1:34238283
HGVS: NM_001281956.2,c.1733A>G,p.His578Arg
Allele change: Missense_H578R

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.