Variant (rsID / SNP)

rs41315247

rs41315247 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SORBS1. Location: chromosome 10, position 97,175,465. The table records no clinical significance for this variant.

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Reference-table entries

SORBS1Not classified

Variant type: intron_variant
Chromosome / position: 10:97175465
HGVS: NM_001384452.1,c.346-4931G>A
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.