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Variant (rsID / SNP)

rs3741280

DSCAML1

rs3741280 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSCAML1. Location: chromosome 11, position 117,403,235. The table records no clinical significance for this variant.

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Reference-table entries

DSCAML1Not classified
Variant type
missense_variant&splice_region_variant
Chromosome / position
11:117403235
HGVS
NM_020693.4,c.514C>A,p.His172Asn
Allele change
Missense_H232N

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.