Variant (rsID / SNP)

rs340138

rs340138 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPR108. Location: chromosome 19, position 6,737,481. The table records no clinical significance for this variant.

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Reference-table entries

GPR108Not classified

Variant type: missense_variant
Chromosome / position: 19:6737481
HGVS: NM_001394717.1,c.107A>G,p.Gln36Arg
Allele change: Missense_Q36R

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.