Variant (rsID / SNP)

rs10264967

rs10264967 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STK31. Location: chromosome 7, position 23,775,477. The table records no clinical significance for this variant.

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Reference-table entries

STK31Not classified

Variant type: missense_variant
Chromosome / position: 7:23775477
HGVS: NM_031414.5,c.804G>T,p.Lys268Asn
Allele change: Missense_K268N

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.