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Variant (rsID / SNP)

rs1992186

GPR55

rs1992186 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPR55. Location: chromosome 2, position 231,775,297. The table records no clinical significance for this variant.

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Reference-table entries

GPR55Not classified
Variant type
synonymous_variant
Chromosome / position
2:231775297
HGVS
NM_005683.4,c.381A>C,p.Leu127Leu
Allele change
Synonymous_L127L

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.