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Variant (rsID / SNP)

rs35937022

GPRC6A

rs35937022 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPRC6A. Location: chromosome 6, position 117,114,290. The table records no clinical significance for this variant.

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Reference-table entries

GPRC6ANot classified
Variant type
missense_variant
Chromosome / position
6:117114290
HGVS
NM_148963.4,c.1796T>C,p.Ile599Thr
Allele change
Missense_I424T

Public references

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