Variant (rsID / SNP)

rs56357614

rs56357614 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to S1PR2. Location: chromosome 19, position 10,335,552. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

S1PR2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:10335552
Cytoband: 19p13.2
HGVS: NM_004230.4(S1PR2):c.30C>A (p.Asn10Lys)
Allele change: Missense_N10K

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.