Variant (rsID / SNP)

rs6654212

rs6654212 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPANXN3. The table records no clinical significance for this variant.

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Reference-table entries

SPANXN3Not classified

Variant type: missense_variant
HGVS: NM_001009609.4,c.129G>C,p.Lys43Asn
Allele change: Missense_K43N

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.