Variant (rsID / SNP)

rs41347648

rs41347648 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYSLTR2. Location: chromosome 13, position 49,281,554. Clinical significance in the table: Uncertain significance.

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Reference-table entries

CYSLTR2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 13:49281554
Cytoband: 13q14.2
HGVS: NM_001308476.3(CYSLTR2):c.601A>G (p.Met201Val)
Allele change: Missense_M201V

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.