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Variant (rsID / SNP)

rs12295710

MRGPRE

rs12295710 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MRGPRE. Location: chromosome 11, position 3,249,984. The table records no clinical significance for this variant.

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Reference-table entries

MRGPRENot classified
Variant type
missense_variant
Chromosome / position
11:3249984
HGVS
NM_001039165.4,c.46G>A,p.Gly16Ser
Allele change
Missense_G16S

Public references

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