Variant (rsID / SNP)

rs35785446

rs35785446 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LSS. Location: chromosome 21, position 47,614,553. The table records no clinical significance for this variant.

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Reference-table entries

LSSNot classified

Variant type: missense_variant
Chromosome / position: 21:47614553
HGVS: NM_001001438.3,c.1840C>T,p.Arg614Trp
Allele change: Missense_R614W

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.