Variant (rsID / SNP)

rs117064827

rs117064827 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to S1PR2. Location: chromosome 19, position 10,334,725. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

S1PR2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 19:10334725
Cytoband: 19p13.2
HGVS: NM_004230.4(S1PR2):c.857T>C (p.Val286Ala)
Allele change: Missense_V286A

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.