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Variant (rsID / SNP)

rs17717241

RAD21L1

rs17717241 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD21L1. Location: chromosome 20, position 1,224,774. The table records no clinical significance for this variant.

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Reference-table entries

RAD21L1Not classified
Variant type
missense_variant
Chromosome / position
20:1224774
HGVS
NM_001136566.3,c.1268A>C,p.His423Pro
Allele change
Missense_H423P

Public references

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