Variant (rsID / SNP)

rs35384259

rs35384259 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MISP. Location: chromosome 19, position 757,752. The table records no clinical significance for this variant.

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Reference-table entries

MISPNot classified

Variant type: missense_variant
Chromosome / position: 19:757752
HGVS: NM_173481.4,c.806G>A,p.Ser269Asn
Allele change: Silent

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.