Variant (rsID / SNP)

rs79031981

rs79031981 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SFSWAP. Location: chromosome 12, position 132,262,713. The table records no clinical significance for this variant.

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Reference-table entries

SFSWAPNot classified

Variant type: missense_variant
Chromosome / position: 12:132262713
HGVS: NM_001261411.2,c.2246C>T,p.Pro749Leu
Allele change: Missense_P749L

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.