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Variant (rsID / SNP)

rs6901250

GPRC6A

rs6901250 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPRC6A. Location: chromosome 6, position 117,114,025. The table records no clinical significance for this variant.

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Reference-table entries

GPRC6ANot classified
Variant type
synonymous_variant
Chromosome / position
6:117114025
HGVS
NM_148963.4,c.2061C>T,p.Ala687Ala
Allele change
Synonymous_A512A

Public references

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