Variant (rsID / SNP)

rs9498038

rs9498038 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SASH1. Location: chromosome 6, position 148,761,603. The table records no clinical significance for this variant.

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Reference-table entries

SASH1Not classified

Variant type: intron_variant
Chromosome / position: 6:148761603
HGVS: NM_015278.5,c.386+60C>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.