Variant (rsID / SNP)

rs142524116

rs142524116 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WASHC4. Location: chromosome 12, position 105,546,149. Clinical significance in the table: Uncertain significance.

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Reference-table entries

WASHC4Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 12:105546149
Cytoband: 12q23.3
HGVS: NM_015275.3(WASHC4):c.2678A>G (p.Asn893Ser)
Allele change: Missense_N894S

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.