Variant (rsID / SNP)

rs786205878

rs786205878 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POR. Location: chromosome 7, position 75,610,416. Clinical significance in the table: Pathogenic.

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Reference-table entries

PORPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Duplication
Chromosome / position: 7:75610416
Cytoband: 7q11.23
HGVS: NM_001395413.1(POR):c.559_571dup (p.Arg191fs)

Associated conditions / phenotypes

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.