Variant (rsID / SNP)

rs28931608

rs28931608 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POR. Location: chromosome 7, position 75,614,497. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

PORPathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 7:75614497
Cytoband: 7q11.23
HGVS: NM_001395413.1(POR):c.1361G>A (p.Arg454His)
Allele change: Missense_R457H

Associated conditions / phenotypes

Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency|Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis

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.