Variant (rsID / SNP)

rs2022923

rs2022923 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SNX31. Location: chromosome 8, position 101,586,133. The table records no clinical significance for this variant.

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Reference-table entries

SNX31Not classified

Variant type: missense_variant
Chromosome / position: 8:101586133
HGVS: NM_152628.4,c.1283A>G,p.Asp428Gly
Allele change: Missense_D329G

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.