Variant (rsID / SNP)

rs202015963

rs202015963 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WASHC5. Location: chromosome 8, position 126,056,870. Clinical significance in the table: Uncertain significance.

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Reference-table entries

WASHC5Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 8:126056870
Cytoband: 8q24.13
HGVS: NM_014846.4(WASHC5):c.2575C>T (p.Arg859Cys)
Allele change: Missense_R859C

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.