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Variant (rsID / SNP)

rs2228956

ASTN1

rs2228956 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ASTN1. Location: chromosome 1, position 176,863,867. The table records no clinical significance for this variant.

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Reference-table entries

ASTN1Not classified
Variant type
missense_variant
Chromosome / position
1:176863867
HGVS
NM_001364856.2,c.2795A>G,p.His932Arg
Allele change
Missense_H924R

Public references

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