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Variant (rsID / SNP)

rs116483940

GPR137

rs116483940 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPR137. Location: chromosome 11, position 64,055,562. The table records no clinical significance for this variant.

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Reference-table entries

GPR137Not classified
Variant type
missense_variant
Chromosome / position
11:64055562
HGVS
NM_001378083.1,c.659C>T,p.Ala220Val
Allele change
Missense_A278V

Public references

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