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Variant (rsID / SNP)

rs4274188

MRGPRX3

rs4274188 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MRGPRX3. Location: chromosome 11, position 18,159,254. The table records no clinical significance for this variant.

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Reference-table entries

MRGPRX3Not classified
Variant type
missense_variant
Chromosome / position
11:18159254
HGVS
NM_001370464.1,c.505A>G,p.Asn169Asp
Allele change
Missense_N169D

Public references

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