Variant (rsID / SNP)

rs373737641

rs373737641 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POR. Location: chromosome 7, position 75,615,731. Clinical significance in the table: Likely benign.

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Reference-table entries

PORLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 7:75615731
Cytoband: 7q11.23
HGVS: NM_001395413.1(POR):c.1966G>A (p.Ala656Thr)
Allele change: Missense_A659T

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.