Variant (rsID / SNP)

rs12150338

rs12150338 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR81. Location: chromosome 17, position 1,634,104. Clinical significance in the table: Benign.

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Reference-table entries

WDR81Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:1634104
Cytoband: 17p13.3
HGVS: NM_001163809.2(WDR81):c.3831C>T (p.Ala1277=)
Allele change: Synonymous_A226A

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.