Variant (rsID / SNP)

rs3742130

rs3742130 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPR18. Location: chromosome 13, position 99,907,341. The table records no clinical significance for this variant.

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Reference-table entries

GPR18Not classified

Variant type: synonymous_variant
Chromosome / position: 13:99907341
HGVS: NM_001098200.2,c.786C>T,p.Asn262Asn
Allele change: Silent

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.