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Variant (rsID / SNP)

rs208696

SASH1

rs208696 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SASH1. Location: chromosome 6, position 148,865,257. The table records no clinical significance for this variant.

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Reference-table entries

SASH1Not classified
Variant type
missense_variant
Chromosome / position
6:148865257
HGVS
NM_015278.5,c.2651A>G,p.Gln884Arg
Allele change
Missense_Q839R

Associated conditions / phenotypes

Missense_Q767R

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.