Variant (rsID / SNP)

rs11159

rs11159 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RNASET2. Location: chromosome 6, position 167,343,141. Clinical significance in the table: Benign.

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Reference-table entries

RNASET2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:167343141
Cytoband: 6q27
HGVS: NM_003730.6(RNASET2):c.706C>T (p.Arg236Trp)
Allele change: Missense_R236W

Associated conditions / phenotypes

Cystic leukoencephalopathy without megalencephaly

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.