Variant (rsID / SNP)

rs10883563

rs10883563 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLF2. Location: chromosome 10, position 102,684,380. The table records no clinical significance for this variant.

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Reference-table entries

SLF2Not classified

Variant type: missense_variant
Chromosome / position: 10:102684380
HGVS: NM_001136123.2,c.1622C>A,p.Ser541Tyr
Allele change: Missense_S541Y

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.