Variant (rsID / SNP)

rs149897775

rs149897775 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WHRN. Location: chromosome 9, position 117,166,177. Clinical significance in the table: Uncertain significance.

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Reference-table entries

WHRNUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 9:117166177
Cytoband: 9q32
HGVS: NM_015404.4(WHRN):c.2417C>T (p.Pro806Leu)
Allele change: Missense_P806L

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.