Variant (rsID / SNP)

rs3742993

rs3742993 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STARD9. Location: chromosome 15, position 42,983,923. The table records no clinical significance for this variant.

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Reference-table entries

STARD9Not classified

Variant type: missense_variant
Chromosome / position: 15:42983923
HGVS: NM_020759.3,c.10147A>G,p.Asn3383Asp
Allele change: Missense_N3383D

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.