Variant (rsID / SNP)

rs736118

rs736118 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STRA6. Location: chromosome 15, position 74,473,739. Clinical significance in the table: Benign.

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Reference-table entries

STRA6Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:74473739
Cytoband: 15q24.1
HGVS: NM_022369.4(STRA6):c.1581G>A (p.Met527Ile)
Allele change: Missense_M542I

Associated conditions / phenotypes

Matthew-Wood syndrome

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.