Variant (rsID / SNP)

rs11557092

rs11557092 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPC24. Location: chromosome 19, position 11,257,018. The table records no clinical significance for this variant.

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Reference-table entries

SPC24Not classified

Variant type: missense_variant
Chromosome / position: 19:11257018
HGVS: NM_001317031.2,c.524A>G,p.Lys175Arg
Allele change: Missense_K175R

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.