Variant (rsID / SNP)

rs370705310

rs370705310 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WASHC5. Location: chromosome 8, position 126,103,910. Clinical significance in the table: Benign.

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Reference-table entries

WASHC5Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 8:126103910
Cytoband: 8q24.13
HGVS: NM_014846.4(WASHC5):c.-178T>C
Allele change: Silent

Associated conditions / phenotypes

Hereditary spastic paraplegia 8

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.