Variant (rsID / SNP)

rs145437203

rs145437203 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR36. Location: chromosome 5, position 110,428,060. Clinical significance in the table: Benign.

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Reference-table entries

WDR36Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:110428060
Cytoband: 5q22.1
HGVS: NM_139281.3(WDR36):c.-95T>C
Allele change: Missense_L25P

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.