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Variant (rsID / SNP)

rs8030587

STARD9

rs8030587 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STARD9. Location: chromosome 15, position 42,981,806. The table records no clinical significance for this variant.

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Reference-table entries

STARD9Not classified
Variant type
missense_variant
Chromosome / position
15:42981806
HGVS
NM_020759.3,c.8030G>A,p.Arg2677His
Allele change
Missense_R2677H

Public references

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