Variant (rsID / SNP)

rs3732083

rs3732083 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CMKLR2, GPR1. Location: chromosome 2, position 207,041,053. The table records no clinical significance for this variant.

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Reference-table entries

CMKLR2Not classified

Variant type: missense_variant
Chromosome / position: 2:207041053
HGVS: NM_001098199.2,c.919A>G,p.Ile307Val
Allele change: Missense_I307V

Associated conditions / phenotypes

Missense_I307V

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.