Variant (rsID / SNP)

rs192189247

rs192189247 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STEAP1B. Location: chromosome 7, position 22,532,321. The table records no clinical significance for this variant.

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Reference-table entries

STEAP1BNot classified

Variant type: missense_variant
Chromosome / position: 7:22532321
HGVS: NM_001164460.2,c.625A>G,p.Ile209Val
Allele change: Missense_I190V

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.